Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271594.1 | 1719 | Missense Mutation | ATT,GTT | I326V | NP_001258523.1 |
NM_144665.3 | 1719 | Missense Mutation | ATT,GTT | I465V | NP_653266.2 |
XM_011542614.1 | 1719 | Missense Mutation | ATT,GTT | I442V | XP_011540916.1 |