| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018365.2 | 1459 | Missense Mutation | GTG,TTG | V432L | NP_060835.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286449.1 | 1459 | Intron | NP_001273378.1 | ||
| NM_198524.2 | 1459 | Intron | NP_940926.1 | ||
| XM_005254359.4 | 1459 | Intron | XP_005254416.1 | ||
| XM_005254361.3 | 1459 | Intron | XP_005254418.1 | ||
| XM_011521530.2 | 1459 | Intron | XP_011519832.1 | ||
| XM_017022160.1 | 1459 | Intron | XP_016877649.1 | ||
| XM_017022161.1 | 1459 | Intron | XP_016877650.1 | ||
| XM_017022162.1 | 1459 | Intron | XP_016877651.1 | ||
| XM_017022163.1 | 1459 | Intron | XP_016877652.1 | ||
| XM_017022164.1 | 1459 | Intron | XP_016877653.1 | ||
| XM_017022166.1 | 1459 | Intron | XP_016877655.1 | ||
| XM_017022167.1 | 1459 | Intron | XP_016877656.1 |