| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001185063.2 | 2472 | Intron | NP_001171992.1 | ||
| NM_007131.4 | 2472 | Missense Mutation | CGG,TGG | R181W | NP_009062.2 |
| XM_005262469.1 | 2472 | Missense Mutation | CGG,TGG | R181W | XP_005262526.1 |
| XM_005262471.3 | 2472 | UTR 5 | XP_005262528.1 | ||
| XM_011531391.1 | 2472 | Missense Mutation | CGG,TGG | R181W | XP_011529693.1 |
| XM_011531395.2 | 2472 | Silent Mutation | ACC,ACT | T61T | XP_011529697.1 |
| XM_011531396.2 | 2472 | Missense Mutation | CGG,TGG | R13W | XP_011529698.1 |
| XM_011531397.2 | 2472 | Silent Mutation | ACC,ACT | T40T | XP_011529699.1 |
| XM_017029818.1 | 2472 | Silent Mutation | ACC,ACT | T65T | XP_016885307.1 |
| XM_017029819.1 | 2472 | Silent Mutation | ACC,ACT | T77T | XP_016885308.1 |
| XM_017029820.1 | 2472 | Silent Mutation | ACC,ACT | T40T | XP_016885309.1 |