Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022475.2 | 754 | Missense Mutation | CGC,TGC | R69C | NP_071920.1 |
XM_005263178.4 | 754 | Missense Mutation | CGC,TGC | R69C | XP_005263235.1 |
XM_006714288.3 | 754 | Missense Mutation | CGC,TGC | R69C | XP_006714351.1 |