| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001101667.1 | 576 | Intron | NP_001095137.1 | ||
| NM_003501.2 | 576 | Intron | NP_003492.2 | ||
| XM_005248011.4 | 576 | Intron | XP_005248068.1 | ||
| XM_005248013.3 | 576 | Intron | XP_005248070.1 | ||
| XM_011513565.2 | 576 | Intron | XP_011511867.1 | ||
| XM_011513566.1 | 576 | Intron | XP_011511868.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152544.2 | 576 | Missense Mutation | CGT,TGT | R177C | NP_689757.2 |
| XM_005247950.3 | 576 | UTR 5 | XP_005248007.1 | ||
| XM_011513406.2 | 576 | Missense Mutation | CGT,TGT | R177C | XP_011511708.1 |
| XM_011513407.2 | 576 | Missense Mutation | CGT,TGT | R177C | XP_011511709.1 |
| XM_011513408.1 | 576 | UTR 5 | XP_011511710.1 | ||
| XM_011513409.2 | 576 | UTR 5 | XP_011511711.1 | ||
| XM_011513410.2 | 576 | Missense Mutation | CGT,TGT | R177C | XP_011511712.1 |
| XM_017007811.1 | 576 | Missense Mutation | CGT,TGT | R177C | XP_016863300.1 |