Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152762.2 | 1351 | Missense Mutation | CGC,TGC | R374C | NP_689975.2 |
XM_011544887.2 | 1351 | Missense Mutation | CGC,TGC | R374C | XP_011543189.1 |
XM_011544888.2 | 1351 | Missense Mutation | CGC,TGC | R238C | XP_011543190.1 |