ENST00000301761.7:c.426C>G
MANE Select
|
ENSP00000301761.3:p.Asp142Glu
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|
ENST00000301761.6:c.426C>G
|
ENSP00000301761.2:p.Asp142Glu
|
|
ENST00000359614.9:c.*134C>G
|
ENSP00000352630.5:n.*134C>G
|
|
ENST00000536670.5:n.396+7883C>G
|
|
|
ENST00000537782.5:c.*72C>G
|
ENSP00000469951.1:n.*72C>G
|
|
ENST00000538594.5:c.370+7883C>G
|
ENSP00000440939.1:n.370+7883C>G
|
|
ENST00000541135.5:c.377+7876C>G
|
ENSP00000443130.1:n.377+7876C>G
|
|
ENST00000542074.1:c.*5C>G
|
ENSP00000469670.1:n.*5C>G
|
|
ENST00000542794.5:c.*428C>G
|
ENSP00000439983.1:n.*428C>G
|
|
ENST00000543044.2:c.390C>G
|
ENSP00000440219.1:p.Asp130Glu
|
|
ENST00000543265.1:c.*49C>G
|
ENSP00000443660.1:n.*49C>G
|
|
ENST00000544025.5:n.465+7883C>G
|
|
|
ENST00000544801.5:c.370+7883C>G
|
ENSP00000442581.1:n.370+7883C>G
|
|
ENST00000544880.1:n.374+7883C>G
|
|
|
NM_017841.2:c.426C>G , LRG_519t1:c.426C>G
|
NP_060311.1:p.Asp142Glu
|
|
NM_017841.4:c.426C>G
MANE Select
|
NP_060311.1:p.Asp142Glu
|
|