Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001134233.1 | 918 | Intron | NP_001127705.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001013661.1 | 918 | Missense Mutation | CAT,CGT | H261R | NP_001013683.1 |