Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002275.3 | 1477 | Missense Mutation | CGC,TGC | R407C | NP_002266.2 |
XM_011524784.2 | 1477 | Missense Mutation | CGC,TGC | R414C | XP_011523086.1 |
XM_017024614.1 | 1477 | Missense Mutation | CGC,TGC | R414C | XP_016880103.1 |