Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016622.3 | 81 | Missense Mutation | GCT,GGT | A8G | NP_057706.2 |
NM_145644.2 | 81 | Missense Mutation | GCT,GGT | A8G | NP_663619.1 |
XM_005264361.2 | 81 | Intron | XP_005264418.1 |