Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001938.3 | 146 | Missense Mutation | CGG,TGG | R5W | NP_001001938.1 |
NM_001142413.1 | 146 | Missense Mutation | CGG,TGG | R5W | NP_001135885.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005226.3 | 146 | Intron | NP_005217.2 |