| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014440.2 | 712 | Missense Mutation | CCT,GCT | P101A | NP_055255.1 |
| XM_005263639.2 | 712 | Missense Mutation | CCT,GCT | P101A | XP_005263696.1 |
| XM_011510965.1 | 712 | Missense Mutation | CCT,GCT | P101A | XP_011509267.1 |
| XM_017003806.1 | 712 | Missense Mutation | CCT,GCT | P101A | XP_016859295.1 |