ENST00000219596.6:c.1530T=
MANE Select
|
ENSP00000219596.1:p.Asp510=
|
|
ENST00000219596.5:c.1530T=
|
ENSP00000219596.1:p.Asp510=
|
|
ENST00000339854.8:c.990T=
|
ENSP00000339639.4:p.Asp330=
|
|
ENST00000536379.5:c.897T=
|
ENSP00000445079.1:p.Asp299=
|
|
ENST00000536980.5:c.897T=
|
ENSP00000444178.1:p.Asp299=
|
|
ENST00000537682.5:c.1530T=
|
ENSP00000438611.1:p.Asp510=
|
|
ENST00000538326.5:c.*155T=
|
ENSP00000437486.1:n.*155T=
|
|
ENST00000539145.5:c.451T=
|
ENSP00000444471.1:n.451T=
|
|
ENST00000539154.1:n.895T=
|
|
|
ENST00000541159.5:c.897T=
|
ENSP00000438711.1:p.Asp299=
|
|
ENST00000542898.5:c.1623T=
|
ENSP00000444615.1:p.Asp541=
|
|
ENST00000570511.5:c.1084T=
|
ENSP00000458312.1:n.1084T=
|
|
ENST00000572244.5:c.278-526T=
|
ENSP00000461186.1:n.278-526T=
|
|
ENST00000574583.5:c.451T=
|
ENSP00000460269.1:n.451T=
|
|
ENST00000576315.5:c.451T=
|
ENSP00000460551.1:n.451T=
|
|
ENST00000621655.1:c.897T=
|
ENSP00000481436.1:p.Asp299=
|
|
NM_000243.2:c.1530T= , LRG_190t1:c.1530T=
|
NP_000234.1:p.Asp510=
|
|
NM_001198536.1:c.897T=
|
NP_001185465.1:p.Asp299=
|
|
XM_017023236.2:c.1527T=
|
XP_016878725.1:p.Asp509=
|
|
XR_001751903.1:n.1719T=
|
|
|
NM_000243.3:c.1530T=
MANE Select
|
NP_000234.1:p.Asp510=
|
|
NM_001198536.2:c.897T=
|
NP_001185465.2:p.Asp299=
|
|