Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303422.1 | 1585 | Missense Mutation | GCT,GTT | A449V | NP_001290351.1 |
NM_004490.2 | 1585 | Missense Mutation | GCT,GTT | A536V | NP_004481.2 |
XM_011511022.2 | 1585 | Intron | XP_011509324.1 | ||
XM_017003899.1 | 1585 | Missense Mutation | GCT,GTT | A336V | XP_016859388.1 |