| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318052.1 | 3077 | Missense Mutation | CGG,TGG | R859W | NP_001304981.1 |
| NM_001318053.1 | 3077 | Intron | NP_001304982.1 | ||
| NM_015689.4 | 3077 | Missense Mutation | CGG,TGG | R859W | NP_056504.3 |
| XM_005249977.3 | 3077 | Missense Mutation | CGG,TGG | R859W | XP_005250034.1 |
| XM_005249979.4 | 3077 | Intron | XP_005250036.1 | ||
| XM_011516052.2 | 3077 | Missense Mutation | CGG,TGG | R859W | XP_011514354.1 |
| XM_011516053.2 | 3077 | Missense Mutation | CGG,TGG | R859W | XP_011514355.1 |
| XM_011516054.2 | 3077 | Missense Mutation | CGG,TGG | R858W | XP_011514356.1 |
| XM_017011989.1 | 3077 | Missense Mutation | CGG,TGG | R859W | XP_016867478.1 |