ID: 84033 | obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (228208044..228378876) | ARHGEF30, RHABDO1, UNC89 | 608616 |
ID: 4633 | myosin light chain 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110910845..110921449, complement) | CMH10, MFM12, MLC-2, MLC-2s/v, MLC-2v, MLC2 | 160781 |
ID: 1158 | creatine kinase, M-type [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45306413..45322875, complement) | CKMM, CPK-M, M-CK | 123310 |
ID: 5913 | receptor associated protein of the synapse [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (47437764..47449136, complement) | CMS11, CMS4C, FADS, FADS2, RAPSYN, RNF205 | 601592 |
ID: 5224 | phosphoglycerate mutase 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (44062727..44065567, complement) | GSD10, PGAM-M, PGAMM | 612931 |
ID: 6345 | sarcalumenin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4189374..4242080, complement) | SAR | 604992 |
ID: 7134 | troponin C1, slow skeletal and cardiac type [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (52451100..52454041, complement) | CMD1Z, CMH13, TN-C, TNC, TNNC | 191040 |
ID: 4625 | myosin heavy chain 7 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (23412740..23435660, complement) | CMD1S, CMH1, CMYO7A, CMYO7B, CMYP7A, CMYP7B, MPD1, MYHCB, SPMD, SPMM | 160760 |
ID: 3270 | histidine rich calcium binding protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49151198..49155396, complement) | | 142705 |
ID: 11259 | filamin A interacting protein 1 like [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (99828811..100114501, complement) | DOC-1, DOC1, GIP130, GIP90 | 612993 |
ID: 126306 | junctional sarcoplasmic reticulum protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2252252..2256417, complement) | JP-45, JP45 | 608743 |
ID: 4656 | myogenin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (203083129..203086012, complement) | MYF4, bHLHc3, myf-4 | 159980 |
ID: 401036 | ankyrin repeat and SOCS box containing 18 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (236193459..236264406, complement) | ASB-18 | |
ID: 4151 | myoglobin [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35606764..35623354, complement) | MYOSB, PVALB | 160000 |
ID: 201140 | dehydrogenase/reductase 7C [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (9771438..9791592, complement) | SDR32C2 | 616161 |
ID: 786 | calcium voltage-gated channel auxiliary subunit gamma 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67044554..67056797) | CACNLG | 114209 |
ID: 136371 | ankyrin repeat and SOCS box containing 10 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (151175698..151187792, complement) | GLC1F | 615054 |
ID: 340359 | kelch like family member 38 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123644442..123653801, complement) | C8ORFK36 | |
ID: 59285 | calcium voltage-gated channel auxiliary subunit gamma 6 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (53991149..54012666) | | 606898 |
ID: 339291 | leucine rich repeat containing 30 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7231089..7232044) | | |