| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001137664.1 | 1202 | Missense Mutation | CGG,TGG | R401W | NP_001131136.1 |
| NM_016238.2 | 1202 | Missense Mutation | CGG,TGG | R401W | NP_057322.2 |
| XM_005253903.3 | 1202 | Missense Mutation | CGG,TGG | R180W | XP_005253960.1 |
| XM_011538454.2 | 1202 | Missense Mutation | CGG,TGG | R381W | XP_011536756.1 |
| XM_017019425.1 | 1202 | Missense Mutation | CGG,TGG | R401W | XP_016874914.1 |
| XM_017019426.1 | 1202 | Missense Mutation | CGG,TGG | R300W | XP_016874915.1 |
| XM_017019427.1 | 1202 | Missense Mutation | CGG,TGG | R300W | XP_016874916.1 |
| XM_017019428.1 | 1202 | Missense Mutation | CGG,TGG | R180W | XP_016874917.1 |