| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_139170.2 | 1624 | Intron | NP_631909.2 | ||
| XM_005255144.3 | 1624 | Intron | XP_005255201.1 | ||
| XM_017022975.1 | 1624 | Intron | XP_016878464.1 | ||
| XM_017022976.1 | 1624 | Intron | XP_016878465.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303450.1 | 1624 | Intron | NP_001290379.1 | ||
| NM_021646.3 | 1624 | Intron | NP_067678.1 | ||
| XM_005255243.3 | 1624 | Intron | XP_005255300.1 | ||
| XM_011522453.2 | 1624 | Silent Mutation | CCA,CCG | P441P | XP_011520755.1 |
| XM_011522454.2 | 1624 | Intron | XP_011520756.1 | ||
| XM_017023121.1 | 1624 | Intron | XP_016878610.1 |