Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003559.4 | 1481 | Missense Mutation | GCT,GTT | A346V | NP_003550.1 |
XM_011525326.2 | 1481 | Missense Mutation | GCT,GTT | A373V | XP_011523628.1 |
XM_011525327.2 | 1481 | Missense Mutation | GCT,GTT | A309V | XP_011523629.1 |
XM_011525329.2 | 1481 | Intron | XP_011523631.1 | ||
XM_011525330.2 | 1481 | Missense Mutation | GCT,GTT | A214V | XP_011523632.1 |
XM_017025196.1 | 1481 | Missense Mutation | GCT,GTT | A282V | XP_016880685.1 |
XM_017025197.1 | 1481 | Missense Mutation | GCT,GTT | A208V | XP_016880686.1 |
XM_017025198.1 | 1481 | Missense Mutation | GCT,GTT | A187V | XP_016880687.1 |
XM_017025199.1 | 1481 | Missense Mutation | GCT,GTT | A178V | XP_016880688.1 |