ENST00000355943.8:c.1024C>G
MANE Select
|
ENSP00000348211.3:p.His342Asp
|
|
ENST00000355943.7:c.1024C>G
|
ENSP00000348211.3:p.His342Asp
|
|
ENST00000447245.6:c.781C>G
|
ENSP00000399717.2:p.His261Asp
|
|
ENST00000502462.6:n.1340C>G
|
|
|
ENST00000504098.1:c.586C>G
|
ENSP00000425708.1:p.His196Asp
|
|
ENST00000509432.1:c.385C>G
|
ENSP00000426604.1:p.His129Asp
|
|
ENST00000513706.2:n.2624C>G
|
|
|
ENST00000513807.5:c.538C>G
|
ENSP00000421134.1:p.His180Asp
|
|
NM_001303249.1:c.781C>G
|
NP_001290178.1:p.His261Asp
|
|
NM_001303250.1:c.751C>G
|
NP_001290179.1:p.His251Asp
|
|
NM_138773.2:c.1024C>G
|
NP_620128.1:p.His342Asp
|
|
NM_001303249.2:c.781C>G
|
NP_001290178.1:p.His261Asp
|
|
NM_001303250.2:c.751C>G
|
NP_001290179.1:p.His251Asp
|
|
NM_138773.3:c.1024C>G
|
NP_620128.1:p.His342Asp
|
|
NR_138151.1:n.1298C>G
|
|
|
NM_138773.4:c.1024C>G
MANE Select
|
NP_620128.1:p.His342Asp
|
|
NM_001303249.3:c.781C>G
|
NP_001290178.1:p.His261Asp
|
|
NM_001303250.3:c.751C>G
|
NP_001290179.1:p.His251Asp
|
|
NR_138151.2:n.1263C>G
|
|
|