ENST00000301761.7:c.448G>A
MANE Select
|
ENSP00000301761.3:p.Glu150Lys
|
|
ENST00000301761.6:c.448G>A
|
ENSP00000301761.2:p.Glu150Lys
|
|
ENST00000536670.5:n.396+7905G>A
|
|
|
ENST00000537782.5:c.*94G>A
|
ENSP00000469951.1:n.*94G>A
|
|
ENST00000538594.5:c.370+7905G>A
|
ENSP00000440939.1:n.370+7905G>A
|
|
ENST00000541135.5:c.377+7898G>A
|
ENSP00000443130.1:n.377+7898G>A
|
|
ENST00000542074.1:c.*27G>A
|
ENSP00000469670.1:n.*27G>A
|
|
ENST00000542794.5:c.*450G>A
|
ENSP00000439983.1:n.*450G>A
|
|
ENST00000543044.2:c.412G>A
|
ENSP00000440219.1:p.Glu138Lys
|
|
ENST00000543265.1:c.*71G>A
|
ENSP00000443660.1:n.*71G>A
|
|
ENST00000544025.5:n.465+7905G>A
|
|
|
ENST00000544801.5:c.370+7905G>A
|
ENSP00000442581.1:n.370+7905G>A
|
|
ENST00000544880.1:n.374+7905G>A
|
|
|
NM_017841.2:c.448G>A , LRG_519t1:c.448G>A
|
NP_060311.1:p.Glu150Lys
|
|
NM_017841.4:c.448G>A
MANE Select
|
NP_060311.1:p.Glu150Lys
|
|