ENST00000375254.8:c.15279C>T
MANE Select
|
ENSP00000364403.3:p.Ser5093=
|
|
ENST00000375224.1:c.2400C>T
|
ENSP00000364372.1:p.Ser800=
|
|
ENST00000375225.7:c.504C>T
|
ENSP00000364373.3:p.Ser168=
|
|
ENST00000375254.7:c.15279C>T
|
ENSP00000364403.3:p.Ser5093=
|
|
ENST00000459947.5:n.3286C>T
|
|
|
NM_020765.2:c.15279C>T
|
NP_065816.2:p.Ser5093=
|
|
XM_011541108.1:c.15432C>T
|
XP_011539410.1:p.Ser5144=
|
|
XM_011541109.1:c.15429C>T
|
XP_011539411.1:p.Ser5143=
|
|
XM_011541110.1:c.15429C>T
|
XP_011539412.1:p.Ser5143=
|
|
XM_011541111.1:c.15429C>T
|
XP_011539413.1:p.Ser5143=
|
|
XM_011541112.1:c.15417C>T
|
XP_011539414.1:p.Ser5139=
|
|
XM_011541113.1:c.15414C>T
|
XP_011539415.1:p.Ser5138=
|
|
XM_011541114.1:c.15414C>T
|
XP_011539416.1:p.Ser5138=
|
|
XM_011541115.1:c.15408C>T
|
XP_011539417.1:p.Ser5136=
|
|
XM_011541116.1:c.15399C>T
|
XP_011539418.1:p.Ser5133=
|
|
XM_011541117.1:c.15348C>T
|
XP_011539419.1:p.Ser5116=
|
|
XM_011541118.1:c.15345C>T
|
XP_011539420.1:p.Ser5115=
|
|
XM_011541119.1:c.15312C>T
|
XP_011539421.1:p.Ser5104=
|
|
XM_011541120.1:c.15309C>T
|
XP_011539422.1:p.Ser5103=
|
|
XM_011541121.1:c.15276C>T
|
XP_011539423.1:p.Ser5092=
|
|
XM_011541108.3:c.15546C>T
|
XP_011539410.2:p.Ser5182=
|
|
XM_011541109.3:c.15543C>T
|
XP_011539411.2:p.Ser5181=
|
|
XM_011541110.3:c.15543C>T
|
XP_011539412.2:p.Ser5181=
|
|
XM_011541111.3:c.15543C>T
|
XP_011539413.2:p.Ser5181=
|
|
XM_011541112.3:c.15531C>T
|
XP_011539414.2:p.Ser5177=
|
|
XM_011541113.3:c.15528C>T
|
XP_011539415.2:p.Ser5176=
|
|
XM_011541114.3:c.15528C>T
|
XP_011539416.2:p.Ser5176=
|
|
XM_011541115.3:c.15522C>T
|
XP_011539417.2:p.Ser5174=
|
|
XM_011541116.3:c.15513C>T
|
XP_011539418.2:p.Ser5171=
|
|
XM_011541117.3:c.15462C>T
|
XP_011539419.2:p.Ser5154=
|
|
XM_011541118.3:c.15459C>T
|
XP_011539420.2:p.Ser5153=
|
|
XM_011541119.3:c.15426C>T
|
XP_011539421.2:p.Ser5142=
|
|
XM_011541120.3:c.15423C>T
|
XP_011539422.2:p.Ser5141=
|
|
XM_011541121.3:c.15390C>T
|
XP_011539423.2:p.Ser5130=
|
|
XM_017000822.2:c.15525C>T
|
XP_016856311.2:p.Ser5175=
|
|
XM_017000823.2:c.15498C>T
|
XP_016856312.2:p.Ser5166=
|
|
XM_017000824.2:c.15444C>T
|
XP_016856313.2:p.Ser5148=
|
|
XM_017000825.2:c.15429C>T
|
XP_016856314.2:p.Ser5143=
|
|
XM_017000826.2:c.15426C>T
|
XP_016856315.2:p.Ser5142=
|
|
XM_017000827.2:c.15411C>T
|
XP_016856316.2:p.Ser5137=
|
|
XM_017000828.2:c.15387C>T
|
XP_016856317.2:p.Ser5129=
|
|
XM_017000829.2:c.15339C>T
|
XP_016856318.2:p.Ser5113=
|
|
XM_017000830.2:c.15288C>T
|
XP_016856319.2:p.Ser5096=
|
|
NM_020765.3:c.15279C>T
MANE Select
|
NP_065816.2:p.Ser5093=
|
|