ENST00000301071.12:c.633C>T
MANE Select
|
ENSP00000301071.7:p.Asp211=
|
|
ENST00000547939.6:c.528C>T
|
ENSP00000450268.2:p.Asp176=
|
|
ENST00000550767.6:c.528C>T
|
ENSP00000446637.1:p.Asp176=
|
|
ENST00000550811.2:n.1666C>T
|
|
|
ENST00000552924.2:c.528C>T
|
ENSP00000448725.2:p.Asp176=
|
|
ENST00000679733.1:c.*89C>T
|
ENSP00000505459.1:n.*89C>T
|
|
ENST00000295766.9:c.633C>T
|
ENSP00000439020.2:p.Asp211=
|
|
ENST00000301071.11:c.633C>T
|
ENSP00000301071.7:p.Asp211=
|
|
ENST00000546918.1:c.*89C>T
|
ENSP00000446613.1:n.*89C>T
|
|
ENST00000547939.5:c.528C>T
|
ENSP00000450268.1:p.Asp176=
|
|
ENST00000550767.5:c.528C>T
|
ENSP00000446637.1:p.Asp176=
|
|
NM_001270399.1:c.633C>T
|
NP_001257328.1:p.Asp211=
|
|
NM_001270400.1:c.528C>T
|
NP_001257329.1:p.Asp176=
|
|
NM_006009.3:c.633C>T
|
NP_006000.2:p.Asp211=
|
|
NM_006009.4:c.633C>T
MANE Select
|
NP_006000.2:p.Asp211=
|
|
NM_001270399.2:c.633C>T
|
NP_001257328.1:p.Asp211=
|
|
NM_001270400.2:c.528C>T
|
NP_001257329.1:p.Asp176=
|
|