Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001324357.1 | 478 | Missense Mutation | ATG,TTG | M103L | NP_001311286.1 |
NM_001324358.1 | 478 | Missense Mutation | ATG,TTG | M49L | NP_001311287.1 |
NM_001324359.1 | 478 | Missense Mutation | ATG,TTG | M7L | NP_001311288.1 |
NM_001324360.1 | 478 | Missense Mutation | ATG,TTG | M7L | NP_001311289.1 |
NM_001324361.1 | 478 | Missense Mutation | ATG,TTG | M49L | NP_001311290.1 |
NM_001324362.1 | 478 | UTR 5 | NP_001311291.1 | ||
NM_001324363.1 | 478 | Missense Mutation | ATG,TTG | M104L | NP_001311292.1 |
NM_018233.3 | 478 | Missense Mutation | ATG,TTG | M104L | NP_060703.3 |