Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001486.3 | 214 | Missense Mutation | ATT,GTT | I50V | NP_001477.2 |
XM_011532763.1 | 214 | Missense Mutation | ATT,GTT | I50V | XP_011531065.1 |
XM_017003796.1 | 214 | Intron | XP_016859285.1 | ||
XM_017003797.1 | 214 | Intron | XP_016859286.1 |