Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016219.4 | 111 | Missense Mutation | GCT,GGT | A13G | NP_057303.2 |
XM_006716945.3 | 111 | Missense Mutation | GCT,GGT | A13G | XP_006717008.1 |
XM_017014239.1 | 111 | Intron | XP_016869728.1 |