| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006822.2 | 782 | Missense Mutation | CGG,TGG | R182W | NP_006813.1 |
| XM_005256334.4 | 782 | Missense Mutation | CGG,TGG | R122W | XP_005256391.1 |
| XM_005256335.3 | 782 | Intron | XP_005256392.1 | ||
| XM_006722271.3 | 782 | Missense Mutation | CGG,TGG | R142W | XP_006722334.1 |
| XM_011523528.2 | 782 | Missense Mutation | CGG,TGG | R165W | XP_011521830.1 |
| XM_017024042.1 | 782 | Intron | XP_016879531.1 | ||
| XM_017024043.1 | 782 | Missense Mutation | CGG,TGG | R122W | XP_016879532.1 |