| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_016208.3 | 716 | Intron | NP_057292.1 | ||
| NM_183057.2 | 716 | Missense Mutation | CGG,TGG | R203W | NP_898880.1 |
| XM_005272323.3 | 716 | Missense Mutation | CGG,TGG | R186W | XP_005272380.1 |
| XM_005272324.3 | 716 | Intron | XP_005272381.1 | ||
| XM_005272325.3 | 716 | Missense Mutation | CGG,TGG | R165W | XP_005272382.1 |
| XM_011517099.1 | 716 | Missense Mutation | CGG,TGG | R165W | XP_011515401.1 |
| XM_011517100.1 | 716 | Intron | XP_011515402.1 | ||
| XM_017013529.1 | 716 | Intron | XP_016869018.1 |