Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308056.1 | 749 | Missense Mutation | GAT,GCT | D176A | NP_001294985.1 |
NM_001308057.1 | 749 | Intron | NP_001294986.1 | ||
NM_001308058.1 | 749 | Intron | NP_001294987.1 | ||
NM_001308059.1 | 749 | Missense Mutation | GAT,GCT | D94A | NP_001294988.1 |
NM_001308060.1 | 749 | Missense Mutation | GAT,GCT | D78A | NP_001294989.1 |
NM_001308061.1 | 749 | Missense Mutation | GAT,GCT | D94A | NP_001294990.1 |
NM_139164.2 | 749 | Missense Mutation | GAT,GCT | D176A | NP_631903.1 |
XM_017009041.1 | 749 | Missense Mutation | GAT,GCT | D78A | XP_016864530.1 |
XM_017009042.1 | 749 | Missense Mutation | GAT,GCT | D78A | XP_016864531.1 |
XM_017009043.1 | 749 | Missense Mutation | GAT,GCT | D78A | XP_016864532.1 |
XM_017009044.1 | 749 | Missense Mutation | GAT,GCT | D94A | XP_016864533.1 |