| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171092.1 | 313 | Intron | NP_001164563.1 | ||
| NM_001171095.1 | 313 | Intron | NP_001164566.1 | ||
| NM_020384.3 | 313 | Intron | NP_065117.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171706.1 | 313 | Intron | NP_001165177.1 | ||
| NM_138382.2 | 313 | Missense Mutation | GCT,GTT | A90V | NP_612391.1 |