| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001159491.1 | 314 | Missense Mutation | GCC,GTC | A64V | NP_001152963.1 |
| NM_015379.4 | 314 | Intron | NP_056194.1 | ||
| XM_017011931.1 | 314 | Silent Mutation | CGC,CGT | R77R | XP_016867420.1 |
| XM_017011932.1 | 314 | Silent Mutation | CGC,CGT | R77R | XP_016867421.1 |
| XM_017011933.1 | 314 | Silent Mutation | CGC,CGT | R77R | XP_016867422.1 |
| XM_017011934.1 | 314 | Silent Mutation | CGC,CGT | R77R | XP_016867423.1 |
| XM_017011935.1 | 314 | Silent Mutation | CGC,CGT | R77R | XP_016867424.1 |
| XM_017011936.1 | 314 | Missense Mutation | GCC,GTC | A64V | XP_016867425.1 |