| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193508.1 | 675 | Missense Mutation | CCT,GCT | P123A | NP_001180437.1 |
| NM_005612.4 | 675 | Missense Mutation | CCT,GCT | P123A | NP_005603.3 |
| XM_011534401.2 | 675 | Missense Mutation | CCT,GCT | P123A | XP_011532703.1 |
| XM_017008527.1 | 675 | Missense Mutation | CCT,GCT | P123A | XP_016864016.1 |