| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015254.3 | 5568 | Missense Mutation | CGG,TGG | R1821W | NP_056069.2 |
| XM_005273458.1 | 5568 | Missense Mutation | CGG,TGG | R1800W | XP_005273515.1 |
| XM_011544457.1 | 5568 | Missense Mutation | CGG,TGG | R1842W | XP_011542759.1 |
| XM_011544458.1 | 5568 | Missense Mutation | CGG,TGG | R1821W | XP_011542760.1 |
| XM_011544459.2 | 5568 | Missense Mutation | CGG,TGG | R1778W | XP_011542761.1 |
| XM_011544460.2 | 5568 | Missense Mutation | CGG,TGG | R1778W | XP_011542762.1 |
| XM_011544461.1 | 5568 | Missense Mutation | CGG,TGG | R1778W | XP_011542763.1 |
| XM_017013257.1 | 5568 | Intron | XP_016868746.1 |