ENST00000369538.4:c.841G>T
|
ENSP00000358551.4:p.Glu281Ter
|
|
ENST00000520113.7:c.853G>T
MANE Select
|
ENSP00000430075.3:p.Glu285Ter
|
|
ENST00000637080.1:c.636G>T
|
ENSP00000489753.1:n.636G>T
|
|
ENST00000639077.1:n.518G>T
|
|
|
ENST00000369538.3:c.940G>T
|
ENSP00000358551.3:p.Glu314Ter
|
|
ENST00000520113.6:c.952G>T
|
ENSP00000430075.2:p.Glu318Ter
|
|
NM_000036.2:c.952G>T
|
NP_000027.2:p.Glu318Ter
|
|
NM_001172626.1:c.940G>T
|
NP_001166097.1:p.Glu314Ter
|
|
NM_000036.3:c.853G>T
MANE Select
|
NP_000027.3:p.Glu285Ter
|
|
NM_001172626.2:c.841G>T
|
NP_001166097.2:p.Glu281Ter
|
|