| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172656.1 | 3264 | Silent Mutation | TAC,TAT | Y830Y | NP_001166127.1 |
| NM_001172657.1 | 3264 | Intron | NP_001166128.1 | ||
| NM_001172658.1 | 3264 | Intron | NP_001166129.1 | ||
| NM_001172659.1 | 3264 | Silent Mutation | TAC,TAT | Y790Y | NP_001166130.1 |
| NM_001172660.1 | 3264 | Intron | NP_001166131.1 | ||
| NM_020972.2 | 3264 | Silent Mutation | TAC,TAT | Y860Y | NP_066023.2 |
| XM_006713900.3 | 3264 | Missense Mutation | CGG,TGG | R964W | XP_006713963.1 |
| XM_006713902.3 | 3264 | UTR 3 | XP_006713965.1 | ||
| XM_006713904.3 | 3264 | Intron | XP_006713967.1 | ||
| XM_011513540.2 | 3264 | Missense Mutation | CGG,TGG | R850W | XP_011511842.1 |
| XM_011513541.2 | 3264 | Intron | XP_011511843.1 | ||
| XM_017008502.1 | 3264 | Missense Mutation | CGG,TGG | R906W | XP_016863991.1 |
| XM_017008503.1 | 3264 | UTR 3 | XP_016863992.1 | ||
| XM_017008504.1 | 3264 | Missense Mutation | ACG,ATG | T935M | XP_016863993.1 |
| XM_017008505.1 | 3264 | Silent Mutation | TAC,TAT | Y746Y | XP_016863994.1 |
| XM_017008506.1 | 3264 | Intron | XP_016863995.1 | ||
| XM_017008507.1 | 3264 | Intron | XP_016863996.1 | ||
| XM_017008508.1 | 3264 | Intron | XP_016863997.1 | ||
| XM_017008509.1 | 3264 | Intron | XP_016863998.1 | ||
| XM_017008510.1 | 3264 | Intron | XP_016863999.1 |