Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002231.2 | 229 | Missense Mutation | GCT,GTT | A63V | NP_001002231.1 |
NM_001256080.1 | 229 | Intron | NP_001243009.1 | ||
NM_005551.4 | 229 | Missense Mutation | GCT,GTT | A63V | NP_005542.1 |