Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_138806.3 | 1062 | Missense Mutation | ATT,GTT | I277V | NP_620161.1 |
NM_138939.2 | 1062 | Intron | NP_620385.1 | ||
NM_138940.2 | 1062 | Intron | NP_620386.1 | ||
NM_170780.2 | 1062 | Missense Mutation | ATT,GTT | I254V | NP_740750.1 |