ENST00000537228.6:c.459A>T
|
ENSP00000445691.1:p.Glu153Asp
|
|
ENST00000543081.6:c.427+354A>T
|
ENSP00000439103.2:n.427+354A>T
|
|
ENST00000544516.6:c.157-524A>T
|
ENSP00000439538.2:n.157-524A>T
|
|
ENST00000545576.2:n.890A>T
|
|
|
ENST00000696246.1:c.444A>T
|
ENSP00000512504.1:p.Glu148Asp
|
|
ENST00000696271.1:n.901A>T
|
|
|
ENST00000696272.1:c.474A>T
|
ENSP00000512515.1:p.Glu158Asp
|
|
ENST00000696273.1:c.522A>T
|
ENSP00000512516.1:p.Glu174Asp
|
|
ENST00000229335.11:c.489A>T
MANE Select
|
ENSP00000229335.6:p.Glu163Asp
|
|
ENST00000229335.10:c.489A>T
|
ENSP00000229335.6:p.Glu163Asp
|
|
ENST00000537228.5:c.459A>T
|
ENSP00000445691.1:p.Glu153Asp
|
|
ENST00000543081.5:c.423+354A>T
|
|
|
ENST00000544516.5:c.153-524A>T
|
|
|
ENST00000545512.1:c.485A>T
|
|
|
ENST00000545576.1:n.815A>T
|
|
|
NM_020661.2:c.489A>T , LRG_17t1:c.489A>T
|
NP_065712.1:p.Glu163Asp
|
|
XM_011520772.1:c.459A>T
|
XP_011519074.1:p.Glu153Asp
|
|
XM_011520773.1:c.427+354A>T
|
XP_011519075.1:n.427+354A>T
|
|
NM_001330343.1:c.459A>T
|
NP_001317272.1:p.Glu153Asp
|
|
NM_020661.3:c.489A>T
|
NP_065712.1:p.Glu163Asp
|
|
XM_011520773.2:c.427+354A>T
|
XP_011519075.1:n.427+354A>T
|
|
NM_020661.4:c.489A>T
MANE Select
|
NP_065712.1:p.Glu163Asp
|
|
NM_001330343.2:c.459A>T
|
NP_001317272.1:p.Glu153Asp
|
|