Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001206426.1 | 336 | Intron | NP_001193355.1 | ||
NM_001206427.1 | 336 | Missense Mutation | CAA,CGA | Q9R | NP_001193356.1 |
NM_032747.3 | 336 | Missense Mutation | CAA,CGA | Q9R | NP_116136.1 |