ENST00000697124.1:n.814G=
|
|
|
ENST00000219596.6:c.1693G=
MANE Select
|
ENSP00000219596.1:p.Glu565=
|
|
ENST00000219596.5:c.1693G=
|
ENSP00000219596.1:p.Glu565=
|
|
ENST00000339854.8:c.1153G=
|
ENSP00000339639.4:p.Glu385=
|
|
ENST00000536379.5:c.1060G=
|
ENSP00000445079.1:p.Glu354=
|
|
ENST00000536980.5:c.1060G=
|
ENSP00000444178.1:p.Glu354=
|
|
ENST00000537682.5:c.1693G=
|
ENSP00000438611.1:p.Glu565=
|
|
ENST00000538326.5:c.*318G=
|
ENSP00000437486.1:n.*318G=
|
|
ENST00000539145.5:c.614G=
|
ENSP00000444471.1:n.614G=
|
|
ENST00000541159.5:c.1060G=
|
ENSP00000438711.1:p.Glu354=
|
|
ENST00000542898.5:c.1786G=
|
ENSP00000444615.1:p.Glu596=
|
|
ENST00000570511.5:c.1165-614G=
|
ENSP00000458312.1:n.1165-614G=
|
|
ENST00000572244.5:c.383G=
|
ENSP00000461186.1:n.383G=
|
|
ENST00000574583.5:c.532-614G=
|
ENSP00000460269.1:n.532-614G=
|
|
ENST00000576315.5:c.532-220G=
|
ENSP00000460551.1:n.532-220G=
|
|
ENST00000621655.1:c.1060G=
|
ENSP00000481436.1:p.Glu354=
|
|
NM_000243.2:c.1693G= , LRG_190t1:c.1693G=
|
NP_000234.1:p.Glu565=
|
|
NM_001198536.1:c.1060G=
|
NP_001185465.1:p.Glu354=
|
|
XM_017023236.2:c.1690G=
|
XP_016878725.1:p.Glu564=
|
|
XR_001751903.1:n.1882G=
|
|
|
NM_000243.3:c.1693G=
MANE Select
|
NP_000234.1:p.Glu565=
|
|
NM_001198536.2:c.1060G=
|
NP_001185465.2:p.Glu354=
|
|