| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001287147.1 | 1069 | Missense Mutation | CCT,GCT | P233A | NP_001274076.1 |
| NM_178176.3 | 1069 | Silent Mutation | CGC,CGG | R300R | NP_835470.1 |
| XM_005250309.3 | 1069 | Missense Mutation | GCC,GGC | A329G | XP_005250366.1 |
| XM_011516126.2 | 1069 | Silent Mutation | CGC,CGG | R264R | XP_011514428.1 |
| XM_011516127.2 | 1069 | Silent Mutation | CGC,CGG | R182R | XP_011514429.1 |