Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007232.2 | 1150 | Missense Mutation | CGC,TGC | R384C | NP_009163.2 |
XM_005260266.3 | 1150 | Missense Mutation | CGC,TGC | R384C | XP_005260323.1 |
XM_017027623.1 | 1150 | Missense Mutation | CGC,TGC | R330C | XP_016883112.1 |