| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271816.1 | 3771 | Missense Mutation | ACC,AGC | T996S | NP_001258745.1 |
| NM_014881.4 | 3771 | Missense Mutation | ACC,AGC | T996S | NP_055696.3 |
| XM_006718090.1 | 3771 | Missense Mutation | ACC,AGC | T996S | XP_006718153.1 |
| XM_011540429.1 | 3771 | Missense Mutation | ACC,AGC | T996S | XP_011538731.1 |