Homo sapiens solute carrier family 26 member 5 (SLC26A5), transcript v - Nucleotide

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Functional Studies of Deafness-Associated Pendrin and Prestin Variants. [Int J Mol Sci. 2024]
Functional Studies of Deafness-Associated Pendrin and Prestin Variants.
Takahashi S, Kojima T, Wasano K, Homma K. Int J Mol Sci. 2024 Feb 27; 25(5). Epub 2024 Feb 27.
The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss. [J Physiol. 2024]
The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss.
Takahashi S, Zhou Y, Cheatham MA, Homma K. J Physiol. 2024 Mar; 602(6):1199-1210. Epub 2024 Mar 3.
Evaluation of inner ear damage by mastoid drilling with measurement of serum prestin (SLC26A5) levels. [Braz J Otorhinolaryngol. 2024]
Evaluation of inner ear damage by mastoid drilling with measurement of serum prestin (SLC26A5) levels.
Baskadem Yilmazer A, Tanrısever O, Alagoz MH, Yilmazer R, Goker AE, Tutar B, Uyar Y. Braz J Otorhinolaryngol. 2024 Mar-Apr; 90(2):101380. Epub 2023 Dec 19.

RefSeq protein product
See the reference protein sequence for prestin isoform b (NP_996766.1).

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Protein sequence from Nucleotide coding region
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Nucleotide