ENST00000368235.8:c.456T>C
MANE Select
|
ENSP00000357218.3:p.Thr152=
|
|
ENST00000467374.2:n.566T>C
|
|
|
ENST00000679369.1:c.345T>C
|
ENSP00000505883.1:p.Thr115=
|
|
ENST00000679649.1:n.495T>C
|
|
|
ENST00000679702.1:c.456T>C
|
ENSP00000505913.1:p.Thr152=
|
|
ENST00000679913.1:n.660T>C
|
|
|
ENST00000680004.1:c.456T>C
|
ENSP00000506275.1:p.Thr152=
|
|
ENST00000680087.1:c.456T>C
|
ENSP00000505907.1:p.Thr152=
|
|
ENST00000680269.1:c.456T>C
|
ENSP00000505899.1:p.Thr152=
|
|
ENST00000680529.1:n.640T>C
|
|
|
ENST00000680661.1:c.456T>C
|
ENSP00000505088.1:p.Thr152=
|
|
ENST00000681054.1:c.456T>C
|
ENSP00000506192.1:p.Thr152=
|
|
ENST00000681523.1:c.456T>C
|
ENSP00000505349.1:p.Thr152=
|
|
ENST00000681645.1:n.495T>C
|
|
|
ENST00000681734.1:c.456T>C
|
ENSP00000506177.1:p.Thr152=
|
|
ENST00000681825.1:n.260T>C
|
|
|
ENST00000681922.1:n.495T>C
|
|
|
ENST00000368233.3:c.456T>C
|
ENSP00000357216.3:p.Thr152=
|
|
ENST00000368234.7:c.456T>C
|
ENSP00000357217.3:p.Thr152=
|
|
ENST00000368235.7:c.456T>C
|
ENSP00000357218.3:p.Thr152=
|
|
ENST00000467374.1:n.365T>C
|
|
|
NM_144772.2:c.456T>C
|
NP_658985.2:p.Thr152=
|
|
XM_017000319.2:c.456T>C
|
XP_016855808.1:p.Thr152=
|
|
NM_144772.3:c.456T>C
MANE Select
|
NP_658985.2:p.Thr152=
|
|