ENST00000369538.4:c.394G>A
|
ENSP00000358551.4:p.Val132Ile
|
|
ENST00000520113.7:c.406G>A
MANE Select
|
ENSP00000430075.3:p.Val136Ile
|
|
ENST00000637080.1:c.409G>A
|
ENSP00000489753.1:p.Val137Ile
|
|
ENST00000639077.1:n.71G>A
|
|
|
ENST00000369538.3:c.493G>A
|
ENSP00000358551.3:p.Val165Ile
|
|
ENST00000485564.3:n.280G>A
|
|
|
ENST00000520113.6:c.505G>A
|
ENSP00000430075.2:p.Val169Ile
|
|
NM_000036.2:c.505G>A
|
NP_000027.2:p.Val169Ile
|
|
NM_001172626.1:c.493G>A
|
NP_001166097.1:p.Val165Ile
|
|
NM_000036.3:c.406G>A
MANE Select
|
NP_000027.3:p.Val136Ile
|
|
NM_001172626.2:c.394G>A
|
NP_001166097.2:p.Val132Ile
|
|