ENST00000301071.12:c.477T>A
MANE Select
|
ENSP00000301071.7:p.Val159=
|
|
ENST00000547939.6:c.372T>A
|
ENSP00000450268.2:p.Val124=
|
|
ENST00000550767.6:c.372T>A
|
ENSP00000446637.1:p.Val124=
|
|
ENST00000550811.2:n.1510T>A
|
|
|
ENST00000552924.2:c.372T>A
|
ENSP00000448725.2:p.Val124=
|
|
ENST00000679733.1:c.500T>A
|
ENSP00000505459.1:p.Leu167Ter
|
|
ENST00000295766.9:c.477T>A
|
ENSP00000439020.2:p.Val159=
|
|
ENST00000301071.11:c.477T>A
|
ENSP00000301071.7:p.Val159=
|
|
ENST00000546918.1:c.629T>A
|
ENSP00000446613.1:p.Leu210Ter
|
|
ENST00000547939.5:c.372T>A
|
ENSP00000450268.1:p.Val124=
|
|
ENST00000550767.5:c.372T>A
|
ENSP00000446637.1:p.Val124=
|
|
NM_001270399.1:c.477T>A
|
NP_001257328.1:p.Val159=
|
|
NM_001270400.1:c.372T>A
|
NP_001257329.1:p.Val124=
|
|
NM_006009.3:c.477T>A
|
NP_006000.2:p.Val159=
|
|
NM_006009.4:c.477T>A
MANE Select
|
NP_006000.2:p.Val159=
|
|
NM_001270399.2:c.477T>A
|
NP_001257328.1:p.Val159=
|
|
NM_001270400.2:c.372T>A
|
NP_001257329.1:p.Val124=
|
|