Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152228.2 | 184 | Missense Mutation | CGC,TGC | R62C | NP_689414.1 |
XM_017002435.1 | 184 | Missense Mutation | CGC,TGC | R62C | XP_016857924.1 |
XM_017002436.1 | 184 | Missense Mutation | CGC,TGC | R62C | XP_016857925.1 |