| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286526.1 | 1056 | Silent Mutation | CCC,CCT | P149P | NP_001273455.1 |
| NM_004765.3 | 1056 | Silent Mutation | CCC,CCT | P149P | NP_004756.2 |
| XM_011545980.2 | 1056 | Silent Mutation | CCC,CCT | P149P | XP_011544282.1 |
| XM_017023885.1 | 1056 | Missense Mutation | CGG,TGG | R153W | XP_016879374.1 |
| XM_017023886.1 | 1056 | Missense Mutation | CGG,TGG | R153W | XP_016879375.1 |
| XM_017023887.1 | 1056 | Missense Mutation | CGG,TGG | R153W | XP_016879376.1 |
| XM_017023888.1 | 1056 | Missense Mutation | CGG,TGG | R153W | XP_016879377.1 |