ENST00000710270.1:c.3166G>A
|
ENSP00000518163.1:p.Glu1056Lys
|
|
ENST00000392723.6:c.2959G>A
|
ENSP00000376484.1:p.Glu987Lys
|
|
ENST00000439756.2:c.3118G>A
|
ENSP00000390156.2:p.Glu1040Lys
|
|
ENST00000703168.1:c.3139G>A
|
ENSP00000515214.1:p.Glu1047Lys
|
|
ENST00000271715.7:c.3118G>A
MANE Select
|
ENSP00000271715.2:p.Glu1040Lys
|
|
ENST00000271715.6:c.3118G>A
|
ENSP00000271715.2:p.Glu1040Lys
|
|
ENST00000358476.7:n.3266G>A
|
|
|
ENST00000368863.6:c.2833G>A
|
ENSP00000357856.2:p.Glu945Lys
|
|
ENST00000392723.5:c.2959G>A
|
ENSP00000376484.1:p.Glu987Lys
|
|
ENST00000409503.5:c.3091G>A
|
ENSP00000386836.1:p.Glu1031Lys
|
|
ENST00000491586.5:c.2986G>A
|
ENSP00000418408.1:p.Glu996Lys
|
|
ENST00000531094.5:c.2932G>A
|
ENSP00000431259.1:p.Glu978Lys
|
|
NM_001194937.1:c.3091G>A
|
NP_001181866.1:p.Glu1031Lys
|
|
NM_001194938.1:c.2932G>A
|
NP_001181867.1:p.Glu978Lys
|
|
NM_015100.3:c.3118G>A
|
NP_055915.2:p.Glu1040Lys
|
|
NM_145796.3:c.2833G>A
|
NP_665739.3:p.Glu945Lys
|
|
NM_207171.2:c.2959G>A
|
NP_997054.1:p.Glu987Lys
|
|
XM_005244999.1:c.3118G>A
|
XP_005245056.1:p.Glu1040Lys
|
|
XM_005245000.3:c.3118G>A
|
XP_005245057.1:p.Glu1040Lys
|
|
XM_005245001.1:c.3118G>A
|
XP_005245058.1:p.Glu1040Lys
|
|
XM_005245005.1:c.2959G>A
|
XP_005245062.1:p.Glu987Lys
|
|
XM_005245006.3:c.2959G>A
|
XP_005245063.1:p.Glu987Lys
|
|
XM_011509330.1:c.3010G>A
|
XP_011507632.1:p.Glu1004Lys
|
|
XM_011509331.1:c.2761G>A
|
XP_011507633.1:p.Glu921Lys
|
|
XM_005244999.3:c.3118G>A
|
XP_005245056.1:p.Glu1040Lys
|
|
XM_005245000.4:c.3118G>A
|
XP_005245057.1:p.Glu1040Lys
|
|
XM_005245001.2:c.3118G>A
|
XP_005245058.1:p.Glu1040Lys
|
|
XM_005245005.2:c.2959G>A
|
XP_005245062.1:p.Glu987Lys
|
|
XM_005245006.5:c.2959G>A
|
XP_005245063.1:p.Glu987Lys
|
|
XM_017000744.1:c.3139G>A
|
XP_016856233.1:p.Glu1047Lys
|
|
XM_017000745.2:c.3091G>A
|
XP_016856234.1:p.Glu1031Lys
|
|
XM_017000746.1:c.3091G>A
|
XP_016856235.1:p.Glu1031Lys
|
|
XM_017000748.1:c.2959G>A
|
XP_016856237.1:p.Glu987Lys
|
|
XM_017000749.1:c.2959G>A
|
XP_016856238.1:p.Glu987Lys
|
|
XM_024454305.1:c.2992G>A
|
XP_024310073.1:p.Glu998Lys
|
|
XM_024454306.1:c.1918G>A
|
XP_024310074.1:p.Glu640Lys
|
|
XR_002959801.1:n.2973G>A
|
|
|
NM_015100.4:c.3118G>A
MANE Select
|
NP_055915.2:p.Glu1040Lys
|
|
NM_001194937.2:c.3091G>A
|
NP_001181866.1:p.Glu1031Lys
|
|
NM_001194938.2:c.2932G>A
|
NP_001181867.1:p.Glu978Lys
|
|
NM_145796.4:c.2833G>A
|
NP_665739.3:p.Glu945Lys
|
|