| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143957.2 | 1564 | Missense Mutation | CCT,GCT | P226A | NP_001137429.1 |
| NM_030784.3 | 1564 | Missense Mutation | CCT,GCT | P226A | NP_110411.1 |
| XM_006715570.3 | 1564 | Missense Mutation | CCT,GCT | P226A | XP_006715633.1 |
| XM_011536153.2 | 1564 | Missense Mutation | CCT,GCT | P226A | XP_011534455.1 |
| XM_011536154.2 | 1564 | Missense Mutation | CCT,GCT | P226A | XP_011534456.1 |
| XM_011536155.2 | 1564 | Missense Mutation | CCT,GCT | P226A | XP_011534457.1 |
| XM_011536157.2 | 1564 | Missense Mutation | CCT,GCT | P226A | XP_011534459.1 |
| XM_011536159.2 | 1564 | Missense Mutation | CCT,GCT | P226A | XP_011534461.1 |
| XM_017011334.1 | 1564 | Missense Mutation | CCT,GCT | P226A | XP_016866823.1 |