| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010863.2 | 521 | Intron | NP_001010863.1 | ||
| NM_001288740.1 | 521 | Intron | NP_001275669.1 | ||
| NM_001288741.1 | 521 | Intron | NP_001275670.1 | ||
| NM_001288742.1 | 521 | Missense Mutation | GGC,GTC | G90V | NP_001275671.1 |
| NM_001288743.1 | 521 | Missense Mutation | GCC,TCC | A153S | NP_001275672.1 |
| XM_011539378.2 | 521 | Intron | XP_011537680.1 | ||
| XM_011539379.1 | 521 | Intron | XP_011537681.1 | ||
| XM_011539380.1 | 521 | Intron | XP_011537682.1 | ||
| XM_011539382.1 | 521 | Intron | XP_011537684.1 | ||
| XM_011539383.2 | 521 | Missense Mutation | TGG,TGT | W100C | XP_011537685.1 |
| XM_011539384.1 | 521 | Intron | XP_011537686.1 | ||
| XM_011539385.1 | 521 | Intron | XP_011537687.1 | ||
| XM_017015792.1 | 521 | Intron | XP_016871281.1 | ||
| XM_017015793.1 | 521 | Intron | XP_016871282.1 | ||
| XM_017015794.1 | 521 | Intron | XP_016871283.1 | ||
| XM_017015795.1 | 521 | Intron | XP_016871284.1 | ||
| XM_017015796.1 | 521 | Intron | XP_016871285.1 | ||
| XM_017015797.1 | 521 | Intron | XP_016871286.1 |