ENST00000710270.1:c.3017A>T
|
ENSP00000518163.1:p.Glu1006Val
|
|
ENST00000392723.6:c.2810A>T
|
ENSP00000376484.1:p.Glu937Val
|
|
ENST00000439756.2:c.2969A>T
|
ENSP00000390156.2:p.Glu990Val
|
|
ENST00000703168.1:c.2990A>T
|
ENSP00000515214.1:p.Glu997Val
|
|
ENST00000271715.7:c.2969A>T
MANE Select
|
ENSP00000271715.2:p.Glu990Val
|
|
ENST00000271715.6:c.2969A>T
|
ENSP00000271715.2:p.Glu990Val
|
|
ENST00000358476.7:n.3117A>T
|
|
|
ENST00000368863.6:c.2684A>T
|
ENSP00000357856.2:p.Glu895Val
|
|
ENST00000392723.5:c.2810A>T
|
ENSP00000376484.1:p.Glu937Val
|
|
ENST00000409503.5:c.2942A>T
|
ENSP00000386836.1:p.Glu981Val
|
|
ENST00000491586.5:c.2837A>T
|
ENSP00000418408.1:p.Glu946Val
|
|
ENST00000531094.5:c.2783A>T
|
ENSP00000431259.1:p.Glu928Val
|
|
NM_001194937.1:c.2942A>T
|
NP_001181866.1:p.Glu981Val
|
|
NM_001194938.1:c.2783A>T
|
NP_001181867.1:p.Glu928Val
|
|
NM_015100.3:c.2969A>T
|
NP_055915.2:p.Glu990Val
|
|
NM_145796.3:c.2684A>T
|
NP_665739.3:p.Glu895Val
|
|
NM_207171.2:c.2810A>T
|
NP_997054.1:p.Glu937Val
|
|
XM_005244999.1:c.2969A>T
|
XP_005245056.1:p.Glu990Val
|
|
XM_005245000.3:c.2969A>T
|
XP_005245057.1:p.Glu990Val
|
|
XM_005245001.1:c.2969A>T
|
XP_005245058.1:p.Glu990Val
|
|
XM_005245005.1:c.2810A>T
|
XP_005245062.1:p.Glu937Val
|
|
XM_005245006.3:c.2810A>T
|
XP_005245063.1:p.Glu937Val
|
|
XM_011509330.1:c.2861A>T
|
XP_011507632.1:p.Glu954Val
|
|
XM_011509331.1:c.2612A>T
|
XP_011507633.1:p.Glu871Val
|
|
XM_005244999.3:c.2969A>T
|
XP_005245056.1:p.Glu990Val
|
|
XM_005245000.4:c.2969A>T
|
XP_005245057.1:p.Glu990Val
|
|
XM_005245001.2:c.2969A>T
|
XP_005245058.1:p.Glu990Val
|
|
XM_005245005.2:c.2810A>T
|
XP_005245062.1:p.Glu937Val
|
|
XM_005245006.5:c.2810A>T
|
XP_005245063.1:p.Glu937Val
|
|
XM_017000744.1:c.2990A>T
|
XP_016856233.1:p.Glu997Val
|
|
XM_017000745.2:c.2942A>T
|
XP_016856234.1:p.Glu981Val
|
|
XM_017000746.1:c.2942A>T
|
XP_016856235.1:p.Glu981Val
|
|
XM_017000748.1:c.2810A>T
|
XP_016856237.1:p.Glu937Val
|
|
XM_017000749.1:c.2810A>T
|
XP_016856238.1:p.Glu937Val
|
|
XM_024454305.1:c.2843A>T
|
XP_024310073.1:p.Glu948Val
|
|
XM_024454306.1:c.1769A>T
|
XP_024310074.1:p.Glu590Val
|
|
XR_002959801.1:n.2824A>T
|
|
|
NM_015100.4:c.2969A>T
MANE Select
|
NP_055915.2:p.Glu990Val
|
|
NM_001194937.2:c.2942A>T
|
NP_001181866.1:p.Glu981Val
|
|
NM_001194938.2:c.2783A>T
|
NP_001181867.1:p.Glu928Val
|
|
NM_145796.4:c.2684A>T
|
NP_665739.3:p.Glu895Val
|
|