Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136497.2 | 227 | Intron | NP_001129969.1 | ||
NM_001243767.1 | 227 | Missense Mutation | ACC,GCC | T7A | NP_001230696.1 |
NM_152265.4 | 227 | Missense Mutation | ACC,GCC | T7A | NP_689478.1 |