| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172566.1 | 761 | Intron | NP_001166037.1 | ||
| NM_001172567.1 | 761 | Missense Mutation | CGG,TGG | R193W | NP_001166038.1 |
| NM_001172568.1 | 761 | Missense Mutation | CGG,TGG | R148W | NP_001166039.1 |
| NM_001172569.1 | 761 | Intron | NP_001166040.1 | ||
| NM_002468.4 | 761 | Missense Mutation | CGG,TGG | R193W | NP_002459.2 |
| XM_005265172.1 | 761 | Missense Mutation | CGG,TGG | R193W | XP_005265229.1 |
| XM_006713170.1 | 761 | Missense Mutation | CGG,TGG | R148W | XP_006713233.1 |