| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017910.3 | 806 | Missense Mutation | TGG,TGT | W356C | NP_060380.3 |
| XM_005264393.2 | 806 | Missense Mutation | TGG,TGT | W356C | XP_005264450.1 |
| XM_006712037.2 | 806 | Missense Mutation | TGG,TGT | W258C | XP_006712100.1 |
| XM_017004401.1 | 806 | Missense Mutation | TGG,TGT | W258C | XP_016859890.1 |
| XM_017004402.1 | 806 | Intron | XP_016859891.1 | ||
| XM_017004403.1 | 806 | Missense Mutation | TGG,TGT | W120C | XP_016859892.1 |