Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142853.2 | 569 | Missense Mutation | GCT,GGT | A117G | NP_001136325.1 |
NM_001282434.1 | 569 | Missense Mutation | CTA,GTA | L106V | NP_001269363.1 |
NM_018645.5 | 569 | Missense Mutation | GCT,GGT | A119G | NP_061115.2 |