Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004470.1 | 981 | Missense Mutation | GCT,GTT | A330V | NP_001004470.1 |
XM_017016174.1 | 981 | Missense Mutation | GCT,GTT | A300V | XP_016871663.1 |
XM_017016175.1 | 981 | Intron | XP_016871664.1 |