ENST00000271651.8:c.468T>A
MANE Select
|
ENSP00000271651.3:p.Thr156=
|
|
ENST00000443913.2:c.645T>A
|
ENSP00000405083.2:p.Thr215=
|
|
ENST00000480670.2:n.3537T>A
|
|
|
ENST00000676680.1:c.468T>A
|
ENSP00000503270.1:p.Thr156=
|
|
ENST00000676716.1:c.345T>A
|
ENSP00000504737.1:p.Thr115=
|
|
ENST00000676751.1:c.468T>A
|
ENSP00000502964.1:p.Thr156=
|
|
ENST00000676824.1:c.468T>A
|
ENSP00000504176.1:p.Thr156=
|
|
ENST00000676966.1:c.468T>A
|
ENSP00000503723.1:p.Thr156=
|
|
ENST00000676970.1:c.468T>A
|
ENSP00000503832.1:p.Thr156=
|
|
ENST00000677330.1:n.2294T>A
|
|
|
ENST00000677611.1:n.320T>A
|
|
|
ENST00000677887.1:c.510T>A
|
ENSP00000503876.1:p.Thr170=
|
|
ENST00000678275.1:c.*360T>A
|
ENSP00000504796.1:n.*360T>A
|
|
ENST00000678337.1:c.504T>A
|
ENSP00000504759.1:p.Thr168=
|
|
ENST00000678725.1:n.1445T>A
|
|
|
ENST00000679090.1:n.1053T>A
|
|
|
ENST00000679148.1:n.3430T>A
|
|
|
ENST00000679171.1:n.2829T>A
|
|
|
ENST00000679260.1:c.399+1690T>A
|
ENSP00000504534.1:n.399+1690T>A
|
|
ENST00000271651.7:c.468T>A
|
ENSP00000271651.3:p.Thr156=
|
|
ENST00000443913.1:c.645T>A
|
ENSP00000405083.1:p.Thr215=
|
|
ENST00000480670.1:n.308T>A
|
|
|
NM_000396.3:c.468T>A
|
NP_000387.1:p.Thr156=
|
|
NM_000396.4:c.468T>A
MANE Select
|
NP_000387.1:p.Thr156=
|
|