ENST00000216714.8:c.506C=
MANE Select
|
ENSP00000216714.3:p.Thr169=
|
|
ENST00000216714.7:c.506C=
|
ENSP00000216714.3:p.Thr169=
|
|
ENST00000398030.8:c.506C=
|
ENSP00000381111.4:p.Thr169=
|
|
ENST00000438886.1:c.289-3C=
|
|
|
ENST00000553555.5:n.926C=
|
|
|
ENST00000553681.5:c.506C=
|
ENSP00000451327.1:p.Thr169=
|
|
ENST00000554813.5:n.572C=
|
|
|
ENST00000555414.5:c.506C=
|
ENSP00000451979.1:p.Thr169=
|
|
ENST00000555839.5:c.440-21C=
|
ENSP00000452460.1:n.440-21C=
|
|
ENST00000556054.5:c.506C=
|
ENSP00000451170.1:p.Thr169=
|
|
ENST00000557054.1:c.28-66C=
|
ENSP00000452212.2:n.28-66C=
|
|
ENST00000557150.5:c.455C=
|
ENSP00000452418.1:p.Thr152=
|
|
ENST00000557159.5:n.1122C=
|
|
|
ENST00000557365.1:n.586C=
|
|
|
ENST00000557592.5:c.455C=
|
ENSP00000451060.1:p.Thr152=
|
|
NM_001244249.1:c.506C=
|
NP_001231178.1:p.Thr169=
|
|
NM_001641.3:c.506C=
|
NP_001632.2:p.Thr169=
|
|
NM_080648.2:c.506C=
|
NP_542379.1:p.Thr169=
|
|
NM_080649.2:c.506C=
|
NP_542380.1:p.Thr169=
|
|
XM_005267581.3:c.506C=
|
XP_005267638.1:p.Thr169=
|
|
XM_005267582.3:c.455C=
|
XP_005267639.1:p.Thr152=
|
|
NM_001641.4:c.506C=
MANE Select
|
NP_001632.2:p.Thr169=
|
|
NM_001244249.2:c.506C=
|
NP_001231178.1:p.Thr169=
|
|
NM_080648.3:c.506C=
|
NP_542379.1:p.Thr169=
|
|
NM_080649.3:c.506C=
|
NP_542380.1:p.Thr169=
|
|