Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001146314.1 | 716 | Missense Mutation | CGC,TGC | R8C | NP_001139786.1 |
NM_001254753.1 | 716 | Intron | NP_001241682.1 | ||
NM_032750.2 | 716 | Missense Mutation | CGC,TGC | R8C | NP_116139.1 |