Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032832.5 | 1712 | Missense Mutation | GCT,GTT | A463V | NP_116221.3 |
XM_011536194.2 | 1712 | Missense Mutation | GCT,GTT | A431V | XP_011534496.1 |
XM_017011380.1 | 1712 | Intron | XP_016866869.1 |