| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001276351.1 | 1266 | Missense Mutation | AGA,GGA | R345G | NP_001263280.1 |
| NM_001276352.1 | 1266 | UTR 3 | NP_001263281.1 | ||
| XM_011541465.2 | 1266 | Missense Mutation | AGA,GGA | R416G | XP_011539767.1 |
| XM_011541466.2 | 1266 | Missense Mutation | AGA,GGA | R416G | XP_011539768.1 |
| XM_011541467.1 | 1266 | Missense Mutation | AGA,GGA | R403G | XP_011539769.1 |
| XM_011541469.1 | 1266 | Missense Mutation | AGA,GGA | R278G | XP_011539771.1 |
| XM_011541472.1 | 1266 | Intron | XP_011539774.1 | ||
| XM_011541473.2 | 1266 | Intron | XP_011539775.1 | ||
| XM_011541475.1 | 1266 | Intron | XP_011539777.1 | ||
| XM_017001276.1 | 1266 | Missense Mutation | AGA,GGA | R416G | XP_016856765.1 |
| XM_017001277.1 | 1266 | Intron | XP_016856766.1 |