Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000485.2 | 492 | Missense Mutation | CGC,TGC | R153C | NP_000476.1 |
NM_001030018.1 | 492 | Intron | NP_001025189.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_030928.3 | 492 | Intron | NP_112190.2 |