ENST00000692008.1:c.237G>T
MANE Select
|
ENSP00000509398.1:p.Glu79Asp
|
|
ENST00000293308.11:c.237G>T
|
ENSP00000293308.6:p.Glu79Asp
|
|
ENST00000546542.1:c.471G>T
|
ENSP00000450228.1:p.Glu157Asp
|
|
ENST00000546583.5:n.308G>T
|
|
|
ENST00000546826.5:c.237G>T
|
ENSP00000447881.1:p.Glu79Asp
|
|
ENST00000546897.5:c.237G>T
|
ENSP00000447402.1:p.Glu79Asp
|
|
ENST00000548998.5:c.357G>T
|
ENSP00000447040.1:p.Glu119Asp
|
|
ENST00000550170.5:n.300G>T
|
|
|
ENST00000552150.5:c.321G>T
|
ENSP00000449404.1:p.Glu107Asp
|
|
ENST00000552551.5:c.237G>T
|
ENSP00000447566.1:p.Glu79Asp
|
|
NM_001256282.1:c.321G>T
|
NP_001243211.1:p.Glu107Asp
|
|
NM_001256293.1:c.237G>T
|
NP_001243222.1:p.Glu79Asp
|
|
NM_002273.3:c.237G>T
|
NP_002264.1:p.Glu79Asp
|
|
NR_045962.1:n.694G>T
|
|
|
NM_001256282.2:c.321G>T
|
NP_001243211.1:p.Glu107Asp
|
|
NM_001256293.2:c.237G>T
|
NP_001243222.1:p.Glu79Asp
|
|
NM_002273.4:c.237G>T
MANE Select
|
NP_002264.1:p.Glu79Asp
|
|
NR_045962.2:n.688G>T
|
|
|