ENST00000261304.7:c.1509A>T
MANE Select
|
ENSP00000261304.2:p.Glu503Asp
|
|
ENST00000261304.6:c.1509A>T
|
ENSP00000261304.2:p.Glu503Asp
|
|
ENST00000393568.8:c.1440A>T
|
ENSP00000377198.4:p.Glu480Asp
|
|
ENST00000393569.6:c.1431A>T
|
ENSP00000377199.2:p.Glu477Asp
|
|
ENST00000544807.6:c.1341A>T
|
ENSP00000437513.2:p.Glu447Asp
|
|
ENST00000555000.5:c.876A>T
|
ENSP00000450472.1:p.Glu292Asp
|
|
ENST00000555179.1:c.206+2014A>T
|
|
|
ENST00000557316.5:c.*907A>T
|
ENSP00000452314.1:n.*907A>T
|
|
NM_000153.3:c.1509A>T
|
NP_000144.2:p.Glu503Asp
|
|
NM_001201401.1:c.1440A>T
|
NP_001188330.1:p.Glu480Asp
|
|
NM_001201402.1:c.1431A>T
|
NP_001188331.1:p.Glu477Asp
|
|
XM_011536618.1:c.1341A>T
|
XP_011534920.1:p.Glu447Asp
|
|
XM_011536618.2:c.1341A>T
|
XP_011534920.1:p.Glu447Asp
|
|
NM_000153.4:c.1509A>T
MANE Select
|
NP_000144.2:p.Glu503Asp
|
|
NM_001201401.2:c.1440A>T
|
NP_001188330.1:p.Glu480Asp
|
|
NM_001201402.2:c.1431A>T
|
NP_001188331.1:p.Glu477Asp
|
|