ENST00000710270.1:c.2652G>C
|
ENSP00000518163.1:p.Arg884=
|
|
ENST00000392723.6:c.2445G>C
|
ENSP00000376484.1:p.Arg815=
|
|
ENST00000439756.2:c.2604G>C
|
ENSP00000390156.2:p.Arg868=
|
|
ENST00000703168.1:c.2625G>C
|
ENSP00000515214.1:p.Arg875=
|
|
ENST00000271715.7:c.2604G>C
MANE Select
|
ENSP00000271715.2:p.Arg868=
|
|
ENST00000271715.6:c.2604G>C
|
ENSP00000271715.2:p.Arg868=
|
|
ENST00000358476.7:n.2752G>C
|
|
|
ENST00000368863.6:c.2319G>C
|
ENSP00000357856.2:p.Arg773=
|
|
ENST00000392723.5:c.2445G>C
|
ENSP00000376484.1:p.Arg815=
|
|
ENST00000409503.5:c.2577G>C
|
ENSP00000386836.1:p.Arg859=
|
|
ENST00000491586.5:c.2472G>C
|
ENSP00000418408.1:p.Arg824=
|
|
ENST00000529669.1:c.804G>C
|
ENSP00000432295.1:p.Arg268=
|
|
ENST00000531094.5:c.2418G>C
|
ENSP00000431259.1:p.Arg806=
|
|
NM_001194937.1:c.2577G>C
|
NP_001181866.1:p.Arg859=
|
|
NM_001194938.1:c.2418G>C
|
NP_001181867.1:p.Arg806=
|
|
NM_015100.3:c.2604G>C
|
NP_055915.2:p.Arg868=
|
|
NM_145796.3:c.2319G>C
|
NP_665739.3:p.Arg773=
|
|
NM_207171.2:c.2445G>C
|
NP_997054.1:p.Arg815=
|
|
XM_005244999.1:c.2604G>C
|
XP_005245056.1:p.Arg868=
|
|
XM_005245000.3:c.2604G>C
|
XP_005245057.1:p.Arg868=
|
|
XM_005245001.1:c.2604G>C
|
XP_005245058.1:p.Arg868=
|
|
XM_005245005.1:c.2445G>C
|
XP_005245062.1:p.Arg815=
|
|
XM_005245006.3:c.2445G>C
|
XP_005245063.1:p.Arg815=
|
|
XM_011509330.1:c.2496G>C
|
XP_011507632.1:p.Arg832=
|
|
XM_011509331.1:c.2247G>C
|
XP_011507633.1:p.Arg749=
|
|
XR_921760.1:n.2432G>C
|
|
|
XM_005244999.3:c.2604G>C
|
XP_005245056.1:p.Arg868=
|
|
XM_005245000.4:c.2604G>C
|
XP_005245057.1:p.Arg868=
|
|
XM_005245001.2:c.2604G>C
|
XP_005245058.1:p.Arg868=
|
|
XM_005245005.2:c.2445G>C
|
XP_005245062.1:p.Arg815=
|
|
XM_005245006.5:c.2445G>C
|
XP_005245063.1:p.Arg815=
|
|
XM_017000744.1:c.2625G>C
|
XP_016856233.1:p.Arg875=
|
|
XM_017000745.2:c.2577G>C
|
XP_016856234.1:p.Arg859=
|
|
XM_017000746.1:c.2577G>C
|
XP_016856235.1:p.Arg859=
|
|
XM_017000748.1:c.2445G>C
|
XP_016856237.1:p.Arg815=
|
|
XM_017000749.1:c.2445G>C
|
XP_016856238.1:p.Arg815=
|
|
XM_024454305.1:c.2478G>C
|
XP_024310073.1:p.Arg826=
|
|
XM_024454306.1:c.1404G>C
|
XP_024310074.1:p.Arg468=
|
|
XR_002959801.1:n.2459G>C
|
|
|
NM_015100.4:c.2604G>C
MANE Select
|
NP_055915.2:p.Arg868=
|
|
NM_001194937.2:c.2577G>C
|
NP_001181866.1:p.Arg859=
|
|
NM_001194938.2:c.2418G>C
|
NP_001181867.1:p.Arg806=
|
|
NM_145796.4:c.2319G>C
|
NP_665739.3:p.Arg773=
|
|