Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008489.3 | 770 | Missense Mutation | TTC,TTG | F157L | NP_001008489.1 |
NM_001199285.1 | 770 | Missense Mutation | TTC,TTG | F157L | NP_001186214.1 |
NM_001199286.1 | 770 | Missense Mutation | TTC,TTG | F157L | NP_001186215.1 |
NM_001199287.1 | 770 | Missense Mutation | TTC,TTG | F157L | NP_001186216.1 |
NM_001199288.1 | 770 | Missense Mutation | TTC,TTG | F157L | NP_001186217.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199290.1 | 770 | Intron | NP_001186219.1 |