| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040006.1 | 272 | Missense Mutation | CCG,GCG | P16A | NP_001035095.1 |
| NM_006706.3 | 272 | Missense Mutation | CCG,GCG | P16A | NP_006697.2 |
| XM_005268365.2 | 272 | Missense Mutation | CCG,GCG | P16A | XP_005268422.1 |
| XM_017008977.1 | 272 | Missense Mutation | CCG,GCG | P16A | XP_016864466.1 |
| XM_017008978.1 | 272 | Missense Mutation | CCG,GCG | P16A | XP_016864467.1 |
| XM_017008979.1 | 272 | Missense Mutation | CCG,GCG | P16A | XP_016864468.1 |
| XM_017008980.1 | 272 | Missense Mutation | CCG,GCG | P16A | XP_016864469.1 |
| XM_017008981.1 | 272 | Intron | XP_016864470.1 | ||
| XM_017008982.1 | 272 | Intron | XP_016864471.1 | ||
| XM_017008983.1 | 272 | Intron | XP_016864472.1 | ||
| XM_017008984.1 | 272 | Missense Mutation | CCG,GCG | P16A | XP_016864473.1 |
| XM_017008985.1 | 272 | Missense Mutation | CCG,GCG | P16A | XP_016864474.1 |