Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080554.2 | 663 | Missense Mutation | GCA,GTA | A142V | NP_001074023.1 |
NM_001080555.2 | 663 | Missense Mutation | GCA,GTA | A142V | NP_001074024.1 |
NM_001206842.1 | 663 | Intron | NP_001193771.1 | ||
NM_001206843.1 | 663 | Missense Mutation | GCA,GTA | A129V | NP_001193772.1 |
NM_001206845.1 | 663 | Intron | NP_001193774.1 | ||
NM_031289.3 | 663 | Intron | NP_112579.2 | ||
NM_153823.3 | 663 | Intron | NP_722545.2 | ||
XM_005253493.2 | 663 | Missense Mutation | GCA,GTA | A166V | XP_005253550.1 |
XM_005253495.1 | 663 | Missense Mutation | GCA,GTA | A166V | XP_005253552.1 |
XM_011520858.1 | 663 | Missense Mutation | GCA,GTA | A166V | XP_011519160.1 |
XM_011520859.1 | 663 | Missense Mutation | GCA,GTA | A142V | XP_011519161.1 |
XM_011520860.1 | 663 | Missense Mutation | GCA,GTA | A166V | XP_011519162.1 |
XM_011520861.1 | 663 | Intron | XP_011519163.1 | ||
XM_011520862.1 | 663 | Missense Mutation | GCA,GTA | A142V | XP_011519164.1 |
XM_011520863.1 | 663 | Intron | XP_011519165.1 |