Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000233.3 | 1811 | Missense Mutation | CGC,TGC | R581C | NP_000224.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198593.1 | 1811 | Intron | NP_001185522.1 | ||
NM_001198594.1 | 1811 | Intron | NP_001185523.1 | ||
NM_172311.2 | 1811 | Intron | NP_758515.1 |