Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_182577.2 | 458 | Missense Mutation | CGC,TGC | R218C | NP_872383.1 |
XM_005259545.4 | 458 | Missense Mutation | CGC,TGC | R110C | XP_005259602.1 |
XM_017026671.1 | 458 | Missense Mutation | CGC,TGC | R110C | XP_016882160.1 |