ENST00000369538.4:c.1232T>A
|
ENSP00000358551.4:p.Val411Glu
|
|
ENST00000520113.7:c.1244T>A
MANE Select
|
ENSP00000430075.3:p.Val415Glu
|
|
ENST00000637080.1:c.1027T>A
|
ENSP00000489753.1:n.1027T>A
|
|
ENST00000639077.1:n.909T>A
|
|
|
ENST00000369538.3:c.1331T>A
|
ENSP00000358551.3:p.Val444Glu
|
|
ENST00000520113.6:c.1343T>A
|
ENSP00000430075.2:p.Val448Glu
|
|
NM_000036.2:c.1343T>A
|
NP_000027.2:p.Val448Glu
|
|
NM_001172626.1:c.1331T>A
|
NP_001166097.1:p.Val444Glu
|
|
NM_000036.3:c.1244T>A
MANE Select
|
NP_000027.3:p.Val415Glu
|
|
NM_001172626.2:c.1232T>A
|
NP_001166097.2:p.Val411Glu
|
|