Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005567.2 | 269 | Intron | NP_001005567.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004757.2 | 269 | Missense Mutation | CAC,CGC | H60R | NP_001004757.1 |