ENST00000261304.7:c.573T>G
MANE Select
|
ENSP00000261304.2:p.Asp191Glu
|
|
ENST00000261304.6:c.573T>G
|
ENSP00000261304.2:p.Asp191Glu
|
|
ENST00000393568.8:c.504T>G
|
ENSP00000377198.4:p.Asp168Glu
|
|
ENST00000393569.6:c.495T>G
|
ENSP00000377199.2:p.Asp165Glu
|
|
ENST00000474294.6:n.563T>G
|
|
|
ENST00000544807.6:c.405T>G
|
ENSP00000437513.2:p.Asp135Glu
|
|
ENST00000554372.5:c.*322T>G
|
ENSP00000451884.1:n.*322T>G
|
|
ENST00000554916.5:n.452T>G
|
|
|
ENST00000556261.5:n.274T>G
|
|
|
ENST00000557316.5:c.573T>G
|
ENSP00000452314.1:p.Asp191Glu
|
|
ENST00000622264.4:c.563T>G
|
|
|
NM_000153.3:c.573T>G
|
NP_000144.2:p.Asp191Glu
|
|
NM_001201401.1:c.504T>G
|
NP_001188330.1:p.Asp168Glu
|
|
NM_001201402.1:c.495T>G
|
NP_001188331.1:p.Asp165Glu
|
|
XM_011536618.1:c.405T>G
|
XP_011534920.1:p.Asp135Glu
|
|
XM_011536618.2:c.405T>G
|
XP_011534920.1:p.Asp135Glu
|
|
NM_000153.4:c.573T>G
MANE Select
|
NP_000144.2:p.Asp191Glu
|
|
NM_001201401.2:c.504T>G
|
NP_001188330.1:p.Asp168Glu
|
|
NM_001201402.2:c.495T>G
|
NP_001188331.1:p.Asp165Glu
|
|