ENST00000710270.1:c.2700T>A
|
ENSP00000518163.1:p.Ala900=
|
|
ENST00000392723.6:c.2493T>A
|
ENSP00000376484.1:p.Ala831=
|
|
ENST00000439756.2:c.2652T>A
|
ENSP00000390156.2:p.Ala884=
|
|
ENST00000703168.1:c.2673T>A
|
ENSP00000515214.1:p.Ala891=
|
|
ENST00000271715.7:c.2652T>A
MANE Select
|
ENSP00000271715.2:p.Ala884=
|
|
ENST00000271715.6:c.2652T>A
|
ENSP00000271715.2:p.Ala884=
|
|
ENST00000358476.7:n.2800T>A
|
|
|
ENST00000368863.6:c.2367T>A
|
ENSP00000357856.2:p.Ala789=
|
|
ENST00000392723.5:c.2493T>A
|
ENSP00000376484.1:p.Ala831=
|
|
ENST00000409503.5:c.2625T>A
|
ENSP00000386836.1:p.Ala875=
|
|
ENST00000491586.5:c.2520T>A
|
ENSP00000418408.1:p.Ala840=
|
|
ENST00000529669.1:c.852T>A
|
ENSP00000432295.1:p.Ala284=
|
|
ENST00000531094.5:c.2466T>A
|
ENSP00000431259.1:p.Ala822=
|
|
NM_001194937.1:c.2625T>A
|
NP_001181866.1:p.Ala875=
|
|
NM_001194938.1:c.2466T>A
|
NP_001181867.1:p.Ala822=
|
|
NM_015100.3:c.2652T>A
|
NP_055915.2:p.Ala884=
|
|
NM_145796.3:c.2367T>A
|
NP_665739.3:p.Ala789=
|
|
NM_207171.2:c.2493T>A
|
NP_997054.1:p.Ala831=
|
|
XM_005244999.1:c.2652T>A
|
XP_005245056.1:p.Ala884=
|
|
XM_005245000.3:c.2652T>A
|
XP_005245057.1:p.Ala884=
|
|
XM_005245001.1:c.2652T>A
|
XP_005245058.1:p.Ala884=
|
|
XM_005245005.1:c.2493T>A
|
XP_005245062.1:p.Ala831=
|
|
XM_005245006.3:c.2493T>A
|
XP_005245063.1:p.Ala831=
|
|
XM_011509330.1:c.2544T>A
|
XP_011507632.1:p.Ala848=
|
|
XM_011509331.1:c.2295T>A
|
XP_011507633.1:p.Ala765=
|
|
XM_005244999.3:c.2652T>A
|
XP_005245056.1:p.Ala884=
|
|
XM_005245000.4:c.2652T>A
|
XP_005245057.1:p.Ala884=
|
|
XM_005245001.2:c.2652T>A
|
XP_005245058.1:p.Ala884=
|
|
XM_005245005.2:c.2493T>A
|
XP_005245062.1:p.Ala831=
|
|
XM_005245006.5:c.2493T>A
|
XP_005245063.1:p.Ala831=
|
|
XM_017000744.1:c.2673T>A
|
XP_016856233.1:p.Ala891=
|
|
XM_017000745.2:c.2625T>A
|
XP_016856234.1:p.Ala875=
|
|
XM_017000746.1:c.2625T>A
|
XP_016856235.1:p.Ala875=
|
|
XM_017000748.1:c.2493T>A
|
XP_016856237.1:p.Ala831=
|
|
XM_017000749.1:c.2493T>A
|
XP_016856238.1:p.Ala831=
|
|
XM_024454305.1:c.2526T>A
|
XP_024310073.1:p.Ala842=
|
|
XM_024454306.1:c.1452T>A
|
XP_024310074.1:p.Ala484=
|
|
XR_002959801.1:n.2507T>A
|
|
|
NM_015100.4:c.2652T>A
MANE Select
|
NP_055915.2:p.Ala884=
|
|
NM_001194937.2:c.2625T>A
|
NP_001181866.1:p.Ala875=
|
|
NM_001194938.2:c.2466T>A
|
NP_001181867.1:p.Ala822=
|
|
NM_145796.4:c.2367T>A
|
NP_665739.3:p.Ala789=
|
|