| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130136.1 | 642 | Missense Mutation | CCG,GCG | P12A | NP_001123608.1 |
| NM_001130137.1 | 642 | Missense Mutation | CCG,GCG | P12A | NP_001123609.1 |
| NM_001130138.1 | 642 | Missense Mutation | CCG,GCG | P12A | NP_001123610.1 |
| NM_020851.2 | 642 | Missense Mutation | CCG,GCG | P12A | NP_065902.1 |
| XM_011521840.2 | 642 | Missense Mutation | CCG,GCG | P12A | XP_011520142.1 |
| XM_011521841.1 | 642 | Missense Mutation | CCG,GCG | P12A | XP_011520143.1 |
| XM_017022446.1 | 642 | Missense Mutation | CCG,GCG | P12A | XP_016877935.1 |