ENST00000369538.4:c.471C>A
|
ENSP00000358551.4:p.Thr157=
|
|
ENST00000520113.7:c.483C>A
MANE Select
|
ENSP00000430075.3:p.Thr161=
|
|
ENST00000637080.1:c.486C>A
|
ENSP00000489753.1:p.Thr162=
|
|
ENST00000639077.1:n.148C>A
|
|
|
ENST00000369538.3:c.570C>A
|
ENSP00000358551.3:p.Thr190=
|
|
ENST00000485564.3:n.357C>A
|
|
|
ENST00000520113.6:c.582C>A
|
ENSP00000430075.2:p.Thr194=
|
|
NM_000036.2:c.582C>A
|
NP_000027.2:p.Thr194=
|
|
NM_001172626.1:c.570C>A
|
NP_001166097.1:p.Thr190=
|
|
NM_000036.3:c.483C>A
MANE Select
|
NP_000027.3:p.Thr161=
|
|
NM_001172626.2:c.471C>A
|
NP_001166097.2:p.Thr157=
|
|