Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243108.1 | 589 | Missense Mutation | CGT,TGT | R172C | NP_001230037.1 |
NM_002663.4 | 589 | Missense Mutation | CGT,TGT | R172C | NP_002654.3 |
XM_005256696.2 | 589 | Intron | XP_005256753.1 | ||
XM_017024764.1 | 589 | UTR 5 | XP_016880253.1 |