| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001085423.1 | 1380 | Intron | NP_001078892.1 | ||
| NM_001291316.1 | 1380 | Intron | NP_001278245.1 | ||
| NM_001291317.1 | 1380 | Intron | NP_001278246.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_007215.3 | 1380 | Missense Mutation | CTT,TTT | L428F | NP_009146.2 |
| XM_006721651.2 | 1380 | Intron | XP_006721714.1 | ||
| XM_017024072.1 | 1380 | Intron | XP_016879561.1 |