Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001174092.2 | 529 | Intron | NP_001167563.1 | ||
NM_001282302.1 | 529 | Missense Mutation | GCA,GTA | A66V | NP_001269231.1 |
NM_032508.3 | 529 | Missense Mutation | GCA,GTA | A66V | NP_115897.1 |