Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001166598.1 | 1096 | Missense Mutation | CAC,CAG | H341Q | NP_001160070.1 |
NM_052968.4 | 1096 | Missense Mutation | CAC,CAG | H341Q | NP_443200.2 |
XM_017017169.1 | 1096 | Missense Mutation | CAC,CAG | H341Q | XP_016872658.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317086.1 | 1096 | Intron | NP_001304015.1 | ||
NM_003904.4 | 1096 | Intron | NP_003895.1 |