Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002668.2 | 1632 | Intron | NP_002659.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001307979.1 | 1632 | Missense Mutation | CAT,CGT | H442R | NP_001294908.1 |
NM_006150.4 | 1632 | Missense Mutation | CAT,CGT | H510R | NP_006141.2 |