Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001316963.1 | 629 | Intron | NP_001303892.1 | ||
NM_001729.3 | 629 | Missense Mutation | GAT,GGT | D96G | NP_001720.1 |
XM_011532211.1 | 629 | Missense Mutation | GAT,GGT | D96G | XP_011530513.1 |
XM_017008568.1 | 629 | Intron | XP_016864057.1 |