Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001163817.1 | 1586 | Missense Mutation | CGG,TGG | R446W | NP_001157289.1 |
NM_001360.2 | 1586 | Missense Mutation | CGG,TGG | R446W | NP_001351.2 |
XM_011544777.1 | 1586 | UTR 3 | XP_011543079.1 |