| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286354.1 | 2648 | Silent Mutation | CCC,CCT | P693P | NP_001273283.1 |
| NM_001286355.1 | 2648 | Silent Mutation | CCC,CCT | P797P | NP_001273284.1 |
| NM_148963.3 | 2648 | Silent Mutation | CCC,CCT | P868P | NP_683766.2 |
| XM_017010475.1 | 2648 | Silent Mutation | CCC,CCT | P821P | XP_016865964.1 |
| XM_017010476.1 | 2648 | Intron | XP_016865965.1 |