| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130914.1 | 1021 | Silent Mutation | CCA,CCT | P266P | NP_001124386.1 |
| NM_006806.4 | 1021 | Silent Mutation | CCA,CCT | P222P | NP_006797.3 |
| XM_011529441.1 | 1021 | Silent Mutation | CCA,CCT | P276P | XP_011527743.1 |
| XM_017028265.1 | 1021 | Silent Mutation | CCA,CCT | P222P | XP_016883754.1 |
| XM_017028266.1 | 1021 | Silent Mutation | CCA,CCT | P222P | XP_016883755.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001207063.1 | 1021 | Intron | NP_001193992.1 | ||
| NM_001207064.1 | 1021 | Intron | NP_001193993.1 | ||
| NM_001207065.1 | 1021 | Intron | NP_001193994.1 | ||
| NM_001207066.1 | 1021 | Intron | NP_001193995.1 | ||
| NM_001338.4 | 1021 | Intron | NP_001329.1 | ||
| XM_011529476.2 | 1021 | Intron | XP_011527778.1 | ||
| XM_011529477.2 | 1021 | UTR 3 | XP_011527779.1 | ||
| XM_011529478.2 | 1021 | Intron | XP_011527780.1 | ||
| XM_011529479.1 | 1021 | Intron | XP_011527781.1 |