Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021939.3 | 578 | Missense Mutation | CGC,TGC | R85C | NP_068758.3 |
XM_011525099.2 | 578 | Missense Mutation | CGC,TGC | R85C | XP_011523401.1 |
XM_011525100.2 | 578 | Intron | XP_011523402.1 |