Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020778.4 | 342 | Missense Mutation | CGT,GGT | R59G | NP_065829.3 |
XM_017022444.1 | 342 | Missense Mutation | CGT,GGT | R59G | XP_016877933.1 |
XM_017022445.1 | 342 | Missense Mutation | CGT,GGT | R59G | XP_016877934.1 |