|
ENST00000524561.2:n.4203C>G
|
|
|
|
ENST00000526037.6:n.537C>G
|
|
|
|
ENST00000528374.2:c.1193C>G
|
|
|
|
ENST00000529967.6:n.2941C>G
|
|
|
|
ENST00000532220.2:n.3835C>G
|
|
|
|
ENST00000642611.2:n.5935C>G
|
|
|
|
ENST00000644057.2:n.1178C>G
|
|
|
|
ENST00000645004.2:n.2101C>G
|
|
|
|
ENST00000682051.1:n.4764C>G
|
|
|
|
ENST00000682110.1:n.4817C>G
|
|
|
|
ENST00000682140.1:c.*388C>G
|
ENSP00000507829.1:n.*388C>G
|
|
|
ENST00000682185.1:n.5907C>G
|
|
|
|
ENST00000682204.1:c.*2740C>G
|
ENSP00000507094.1:n.*2740C>G
|
|
|
ENST00000682215.1:n.5184C>G
|
|
|
|
ENST00000682288.1:c.*3033C>G
|
ENSP00000507506.1:n.*3033C>G
|
|
|
ENST00000682442.1:n.5037C>G
|
|
|
|
ENST00000682528.1:n.4894C>G
|
|
|
|
ENST00000682673.1:n.4761C>G
|
|
|
|
ENST00000682805.1:n.5222C>G
|
|
|
|
ENST00000682965.1:c.*1024C>G
|
ENSP00000508229.1:n.*1024C>G
|
|
|
ENST00000683093.1:n.5797C>G
|
|
|
|
ENST00000683136.1:c.4485C>G
|
ENSP00000507768.1:p.Thr1495=
|
|
|
ENST00000683153.1:n.4859C>G
|
|
|
|
ENST00000683365.1:n.4919C>G
|
|
|
|
ENST00000683377.1:n.4713C>G
|
|
|
|
ENST00000683456.1:c.*1739C>G
|
ENSP00000508318.1:n.*1739C>G
|
|
|
ENST00000683522.1:n.4899C>G
|
|
|
|
ENST00000683562.1:c.*2667C>G
|
ENSP00000508265.1:n.*2667C>G
|
|
|
ENST00000683693.1:n.6278C>G
|
|
|
|
ENST00000683725.1:c.*67C>G
|
ENSP00000507496.1:n.*67C>G
|
|
|
ENST00000684010.1:n.4812C>G
|
|
|
|
ENST00000684014.1:n.789C>G
|
|
|
|
ENST00000684157.1:n.5802C>G
|
|
|
|
ENST00000684253.1:n.4720C>G
|
|
|
|
ENST00000684288.1:c.*2774C>G
|
ENSP00000507143.1:n.*2774C>G
|
|
|
ENST00000684313.1:n.4249C>G
|
|
|
|
ENST00000684332.1:n.4890C>G
|
|
|
|
ENST00000684371.1:n.4923C>G
|
|
|
|
ENST00000684404.1:n.5845C>G
|
|
|
|
ENST00000684442.1:n.5041C>G
|
|
|
|
ENST00000684555.1:c.*2814C>G
|
ENSP00000507705.1:n.*2814C>G
|
|
|
ENST00000684571.1:c.4443C>G
|
ENSP00000506935.1:p.Thr1481=
|
|
|
ENST00000684593.1:c.*4307C>G
|
ENSP00000507005.1:n.*4307C>G
|
|
|
ENST00000684711.1:c.*2998C>G
|
ENSP00000506841.1:n.*2998C>G
|
|
|
ENST00000302539.9:c.4605C>G
|
ENSP00000303960.4:p.Thr1535=
|
|
|
ENST00000389817.8:c.4602C>G
MANE Select
|
ENSP00000374467.4:p.Thr1534=
|
|
|
ENST00000642271.1:c.4599C>G
|
ENSP00000493749.1:p.Thr1533=
|
|
|
ENST00000642579.1:c.2656C>G
|
|
|
|
ENST00000642611.1:n.5820C>G
|
|
|
|
ENST00000642902.1:c.4384C>G
|
|
|
|
ENST00000643260.1:c.4602C>G
|
ENSP00000494450.1:p.Thr1534=
|
|
|
ENST00000643562.1:c.*2724C>G
|
ENSP00000496124.1:n.*2724C>G
|
|
|
ENST00000643925.1:c.3185+563C>G
|
|
|
|
ENST00000644057.1:n.761C>G
|
|
|
|
ENST00000644484.1:c.*3988C>G
|
ENSP00000493558.1:n.*3988C>G
|
|
|
ENST00000644675.1:c.*2774C>G
|
ENSP00000494567.1:n.*2774C>G
|
|
|
ENST00000644757.1:c.*3203-723C>G
|
ENSP00000495085.1:n.*3203-723C>G
|
|
|
ENST00000644772.1:c.4668C>G
|
ENSP00000494321.1:p.Thr1556=
|
|
|
ENST00000645004.1:n.2295C>G
|
|
|
|
ENST00000645076.1:c.3697C>G
|
|
|
|
ENST00000645417.1:c.1790C>G
|
|
|
|
ENST00000645744.1:c.*4287C>G
|
ENSP00000494564.1:n.*4287C>G
|
|
|
ENST00000645760.1:c.5023C>G
|
|
|
|
ENST00000645884.1:c.*1885C>G
|
ENSP00000495516.1:n.*1885C>G
|
|
|
ENST00000646003.1:c.*2624C>G
|
ENSP00000495259.1:n.*2624C>G
|
|
|
ENST00000646207.1:c.*3439C>G
|
ENSP00000495025.1:n.*3439C>G
|
|
|
ENST00000646276.1:c.*4006C>G
|
ENSP00000496070.1:n.*4006C>G
|
|
|
ENST00000646592.1:c.3908C>G
|
|
|
|
ENST00000646902.1:c.4569C>G
|
ENSP00000494101.1:p.Thr1523=
|
|
|
ENST00000646993.1:c.*3040C>G
|
ENSP00000493720.1:n.*3040C>G
|
|
|
ENST00000647015.1:c.4353C>G
|
ENSP00000495389.1:p.Thr1451=
|
|
|
ENST00000647086.1:c.*4188C>G
|
ENSP00000493677.1:n.*4188C>G
|
|
|
ENST00000647158.1:c.*2889C>G
|
ENSP00000495744.1:n.*2889C>G
|
|
|
ENST00000302539.8:c.4605C>G
|
ENSP00000303960.4:p.Thr1535=
|
|
|
ENST00000389817.7:c.4602C>G
|
ENSP00000374467.3:p.Thr1534=
|
|
|
ENST00000525022.1:n.497C>G
|
|
|
|
ENST00000526037.5:n.362C>G
|
|
|
|
ENST00000526168.5:c.390C>G
|
|
|
|
ENST00000531642.5:c.633C>G
|
|
|
|
NM_000352.4:c.4602C>G
|
NP_000343.2:p.Thr1534=
|
|
|
NM_001287174.1:c.4605C>G
|
NP_001274103.1:p.Thr1535=
|
|
|
XM_011520331.1:c.4602C>G
|
XP_011518633.1:p.Thr1534=
|
|
|
XM_011520333.1:c.3102C>G
|
XP_011518635.1:p.Thr1034=
|
|
|
XR_930890.1:n.4564C>G
|
|
|
|
NM_001351295.1:c.4668C>G
|
NP_001338224.1:p.Thr1556=
|
|
|
NM_001351296.1:c.4602C>G
|
NP_001338225.1:p.Thr1534=
|
|
|
NM_001351297.1:c.4599C>G
|
NP_001338226.1:p.Thr1533=
|
|
|
NR_147094.1:n.4897C>G
|
|
|
|
XM_017018197.2:c.4671C>G
|
XP_016873686.1:p.Thr1557=
|
|
|
XM_017018199.1:c.4668C>G
|
XP_016873688.1:p.Thr1556=
|
|
|
XM_017018202.1:c.3168C>G
|
XP_016873691.1:p.Thr1056=
|
|
|
XM_017018204.1:c.2559C>G
|
XP_016873693.1:p.Thr853=
|
|
|
XM_024448668.1:c.2970C>G
|
XP_024304436.1:p.Thr990=
|
|
|
XR_001747945.2:n.4639C>G
|
|
|
|
XR_001747946.2:n.4570C>G
|
|
|
|
XR_002957189.1:n.6353C>G
|
|
|
|
NM_000352.6:c.4602C>G
MANE Select
|
NP_000343.2:p.Thr1534=
|
|
|
NM_001287174.2:c.4605C>G
|
NP_001274103.1:p.Thr1535=
|
|
|
NM_001351295.2:c.4668C>G
|
NP_001338224.1:p.Thr1556=
|
|
|
NM_001351296.2:c.4602C>G
|
NP_001338225.1:p.Thr1534=
|
|
|
NM_001351297.2:c.4599C>G
|
NP_001338226.1:p.Thr1533=
|
|
|
NR_147094.2:n.4897C>G
|
|
|
|
NM_001287174.3:c.4605C>G
|
NP_001274103.1:p.Thr1535=
|
|
