Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001012507.3 | 713 | Missense Mutation | AGG,GGG | R59G | NP_001012525.1 |
NM_001286524.1 | 713 | Missense Mutation | AGG,GGG | R74G | NP_001273453.1 |
NM_001286525.1 | 713 | Silent Mutation | CCA,CCG | P45P | NP_001273454.1 |
XM_017010845.1 | 713 | Silent Mutation | CCA,CCG | P45P | XP_016866334.1 |