Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_031885.3 | 1416 | Intron | NP_114091.3 | ||
XM_005256080.2 | 1416 | Intron | XP_005256137.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001324357.1 | 1416 | Missense Mutation | CAC,CAG | H415Q | NP_001311286.1 |
NM_001324358.1 | 1416 | Missense Mutation | CAC,CAG | H361Q | NP_001311287.1 |
NM_001324359.1 | 1416 | Missense Mutation | CAC,CAG | H319Q | NP_001311288.1 |
NM_001324360.1 | 1416 | Missense Mutation | CAC,CAG | H319Q | NP_001311289.1 |
NM_001324361.1 | 1416 | Missense Mutation | CAC,CAG | H361Q | NP_001311290.1 |
NM_001324362.1 | 1416 | Missense Mutation | CAC,CAG | H276Q | NP_001311291.1 |
NM_001324363.1 | 1416 | Missense Mutation | CAC,CAG | H378Q | NP_001311292.1 |
NM_018233.3 | 1416 | Missense Mutation | CAC,CAG | H416Q | NP_060703.3 |