Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_153711.3 | 147 | Missense Mutation | CAT,CGT | H32R | NP_714922.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001139444.2 | 147 | Intron | NP_001132916.1 |