ENST00000369538.4:c.22+2007A>T
|
ENSP00000358551.4:n.22+2007A>T
|
|
ENST00000520113.7:c.27A>T
MANE Select
|
ENSP00000430075.3:p.Glu9Asp
|
|
ENST00000637080.1:c.37+1994A>T
|
ENSP00000489753.1:n.37+1994A>T
|
|
ENST00000369538.3:c.121+2007A>T
|
ENSP00000358551.3:n.121+2007A>T
|
|
ENST00000520113.6:c.126A>T
|
ENSP00000430075.2:p.Glu42Asp
|
|
NM_000036.2:c.126A>T
|
NP_000027.2:p.Glu42Asp
|
|
NM_001172626.1:c.121+2007A>T
|
NP_001166097.1:n.121+2007A>T
|
|
NM_000036.3:c.27A>T
MANE Select
|
NP_000027.3:p.Glu9Asp
|
|
NM_001172626.2:c.22+2007A>T
|
NP_001166097.2:n.22+2007A>T
|
|