| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001520.2 | 176 | Silent Mutation | CCC,CCT | P7P | NP_001001520.1 |
| NM_032631.3 | 176 | Silent Mutation | CCC,CCT | P7P | NP_116020.1 |
| XM_011528375.2 | 176 | Intron | XP_011526677.1 | ||
| XM_011528376.2 | 176 | Intron | XP_011526678.1 | ||
| XM_011528377.2 | 176 | Intron | XP_011526679.1 |