| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001114123.2 | 792 | Silent Mutation | CCC,CCG | P192P | NP_001107595.1 |
| NM_001257168.1 | 792 | Intron | NP_001244097.1 | ||
| NM_005229.4 | 792 | Silent Mutation | CCC,CCG | P192P | NP_005220.2 |
| XM_017029339.1 | 792 | Silent Mutation | CCC,CCG | P192P | XP_016884828.1 |