ENST00000271651.8:c.549C>A
MANE Select
|
ENSP00000271651.3:p.Thr183=
|
|
ENST00000443913.2:c.726C>A
|
ENSP00000405083.2:p.Thr242=
|
|
ENST00000480670.2:n.3618C>A
|
|
|
ENST00000676680.1:c.549C>A
|
ENSP00000503270.1:p.Thr183=
|
|
ENST00000676716.1:c.426C>A
|
ENSP00000504737.1:p.Thr142=
|
|
ENST00000676751.1:c.549C>A
|
ENSP00000502964.1:p.Thr183=
|
|
ENST00000676824.1:c.549C>A
|
ENSP00000504176.1:p.Thr183=
|
|
ENST00000676966.1:c.549C>A
|
ENSP00000503723.1:p.Thr183=
|
|
ENST00000676970.1:c.549C>A
|
ENSP00000503832.1:p.Thr183=
|
|
ENST00000677330.1:n.2375C>A
|
|
|
ENST00000677611.1:n.401C>A
|
|
|
ENST00000677887.1:c.591C>A
|
ENSP00000503876.1:p.Thr197=
|
|
ENST00000678275.1:c.*441C>A
|
ENSP00000504796.1:n.*441C>A
|
|
ENST00000678337.1:c.585C>A
|
ENSP00000504759.1:p.Thr195=
|
|
ENST00000678725.1:n.1526C>A
|
|
|
ENST00000679090.1:n.1134C>A
|
|
|
ENST00000679148.1:n.3511C>A
|
|
|
ENST00000679171.1:n.2910C>A
|
|
|
ENST00000679260.1:c.399+1771C>A
|
ENSP00000504534.1:n.399+1771C>A
|
|
ENST00000271651.7:c.549C>A
|
ENSP00000271651.3:p.Thr183=
|
|
ENST00000443913.1:c.726C>A
|
ENSP00000405083.1:p.Thr242=
|
|
ENST00000480670.1:n.389C>A
|
|
|
NM_000396.3:c.549C>A
|
NP_000387.1:p.Thr183=
|
|
NM_000396.4:c.549C>A
MANE Select
|
NP_000387.1:p.Thr183=
|
|