| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001031722.3 | 398 | Intron | NP_001026892.1 | ||
| NM_001190724.2 | 398 | Intron | NP_001177653.1 | ||
| NM_001254952.2 | 398 | Intron | NP_001241881.1 | ||
| NM_001318762.1 | 398 | Intron | NP_001305691.1 | ||
| NM_001318763.1 | 398 | Intron | NP_001305692.1 | ||
| NM_024909.3 | 398 | Intron | NP_079185.2 | ||
| XM_005249415.2 | 398 | Intron | XP_005249472.1 | ||
| XM_011514918.2 | 398 | Intron | XP_011513220.1 | ||
| XM_017011316.1 | 398 | Intron | XP_016866805.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001109938.2 | 398 | Intron | NP_001103408.1 | ||
| NM_001161376.1 | 398 | Silent Mutation | CTG,TTG | L69L | NP_001154848.1 |
| NM_145029.3 | 398 | Intron | NP_659466.2 | ||
| XM_011514384.1 | 398 | Intron | XP_011512686.1 |