| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018948.3 | 1132 | Missense Mutation | CCT,CTT | P290L | NP_061821.1 |
| XM_005263477.2 | 1132 | Missense Mutation | CCT,CTT | P239L | XP_005263534.1 |
| XM_006710697.2 | 1132 | Missense Mutation | CCT,CTT | P290L | XP_006710760.1 |
| XM_011541596.2 | 1132 | Missense Mutation | CCT,CTT | P215L | XP_011539898.1 |