Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136264.1 | 526 | Silent Mutation | AAC,AAT | N124N | NP_001129736.1 |
NM_001136266.1 | 526 | Missense Mutation | CGT,TGT | R121C | NP_001129738.1 |
NM_001136267.1 | 526 | Silent Mutation | AAC,AAT | N114N | NP_001129739.1 |
NM_001136268.1 | 526 | Silent Mutation | AAC,AAT | N64N | NP_001129740.1 |
NM_001136269.1 | 526 | Intron | NP_001129741.1 | ||
NM_014764.3 | 526 | Silent Mutation | AAC,AAT | N146N | NP_055579.1 |