| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142473.1 | 1099 | Missense Mutation | CCA,CGA | P195R | NP_001135945.1 |
| NM_001193338.1 | 1099 | Silent Mutation | GCC,GCG | A263A | NP_001180267.1 |
| NM_005449.4 | 1099 | Missense Mutation | CCA,CGA | P307R | NP_005440.1 |
| XM_005273351.3 | 1099 | Missense Mutation | CCA,CGA | P307R | XP_005273408.1 |
| XM_005273352.4 | 1099 | Missense Mutation | CCA,CGA | P216R | XP_005273409.1 |