Homo sapiens phenylalanyl-tRNA synthetase 2, mitochondrial (FARS2), tr - Nucleotide

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Clinical and molecular characterization of novel FARS2 variants causing neonatal mitochondrial disease. [Mol Genet Metab. 2023]
Clinical and molecular characterization of novel FARS2 variants causing neonatal mitochondrial disease.
Chen W, Rehsi P, Thompson K, Yeo M, Stals K, He L, Schimmel P, Chrzanowska-Lightowlers ZMA, Wakeling E, Taylor RW, et al. Mol Genet Metab. 2023 Nov; 140(3):107657. Epub 2023 Jul 24.
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing. [Neuro Oncol. 2023]
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing.
Demirdizen E, Al-Ali R, Narayanan A, Sun X, Varga JP, Steffl B, Brom M, Krunic D, Schmidt C, Schmidt G, et al. Neuro Oncol. 2023 Jun 2; 25(6):1031-1043.
Two Chinese siblings of combined oxidative phosphorylation deficiency 14 caused by compound heterozygous variants in FARS2. [Eur J Med Res. 2022]
Two Chinese siblings of combined oxidative phosphorylation deficiency 14 caused by compound heterozygous variants in FARS2.
Li L, Ma J, Wang J, Dong L, Liu S. Eur J Med Res. 2022 Sep 26; 27(1):184. Epub 2022 Sep 26.

RefSeq alternative splicing
See 25 reference mRNA sequence splice variants for the FARS2 gene.
RefSeq protein product
See the reference protein sequence for phenylalanine--tRNA ligase, mitochondrial isoform 1 (NP_001361808.1).

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Protein sequence from Nucleotide coding region
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Nucleotide