| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001197327.1 | 262 | Silent Mutation | CCC,CCT | P40P | NP_001184256.1 |
| NM_001318322.1 | 262 | Intron | NP_001305251.1 | ||
| NM_052970.4 | 262 | Silent Mutation | CCC,CCT | P40P | NP_443202.3 |
| XM_011529151.2 | 262 | Intron | XP_011527453.1 | ||
| XM_017027632.1 | 262 | Silent Mutation | CCC,CCT | P40P | XP_016883121.1 |
| XM_017027633.1 | 262 | Silent Mutation | CCC,CCT | P40P | XP_016883122.1 |
| XM_017027634.1 | 262 | Silent Mutation | CCC,CCT | P40P | XP_016883123.1 |
| XM_017027635.1 | 262 | Silent Mutation | CCC,CCT | P40P | XP_016883124.1 |