Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001287593.1 | 838 | Missense Mutation | CGC,TGC | R89C | NP_001274522.1 |
NM_001287594.1 | 838 | Intron | NP_001274523.1 | ||
NM_001288.4 | 838 | Missense Mutation | CGC,TGC | R89C | NP_001279.2 |