ENST00000524561.2:n.4053A>C
|
|
|
ENST00000526037.6:n.387A>C
|
|
|
ENST00000528374.2:c.1043A>C
|
|
|
ENST00000529967.6:n.2791A>C
|
|
|
ENST00000532220.2:n.3685A>C
|
|
|
ENST00000642611.2:n.5785A>C
|
|
|
ENST00000644057.2:n.1028A>C
|
|
|
ENST00000645004.2:n.1951A>C
|
|
|
ENST00000682051.1:n.4614A>C
|
|
|
ENST00000682110.1:n.4667A>C
|
|
|
ENST00000682140.1:c.*238A>C
|
ENSP00000507829.1:n.*238A>C
|
|
ENST00000682185.1:n.5757A>C
|
|
|
ENST00000682204.1:c.*2590A>C
|
ENSP00000507094.1:n.*2590A>C
|
|
ENST00000682215.1:n.5034A>C
|
|
|
ENST00000682288.1:c.*2883A>C
|
ENSP00000507506.1:n.*2883A>C
|
|
ENST00000682442.1:n.4887A>C
|
|
|
ENST00000682528.1:n.4744A>C
|
|
|
ENST00000682673.1:n.4611A>C
|
|
|
ENST00000682805.1:n.5072A>C
|
|
|
ENST00000682965.1:c.*874A>C
|
ENSP00000508229.1:n.*874A>C
|
|
ENST00000683093.1:n.5647A>C
|
|
|
ENST00000683136.1:c.4335A>C
|
ENSP00000507768.1:p.Gly1445=
|
|
ENST00000683153.1:n.4709A>C
|
|
|
ENST00000683365.1:n.4769A>C
|
|
|
ENST00000683377.1:n.4563A>C
|
|
|
ENST00000683456.1:c.*1589A>C
|
ENSP00000508318.1:n.*1589A>C
|
|
ENST00000683522.1:n.4749A>C
|
|
|
ENST00000683562.1:c.*2517A>C
|
ENSP00000508265.1:n.*2517A>C
|
|
ENST00000683693.1:n.6128A>C
|
|
|
ENST00000683725.1:c.4348A>C
|
ENSP00000507496.1:p.Thr1450Pro
|
|
ENST00000684010.1:n.4662A>C
|
|
|
ENST00000684014.1:n.639A>C
|
|
|
ENST00000684157.1:n.5652A>C
|
|
|
ENST00000684253.1:n.4570A>C
|
|
|
ENST00000684288.1:c.*2624A>C
|
ENSP00000507143.1:n.*2624A>C
|
|
ENST00000684313.1:n.4099A>C
|
|
|
ENST00000684332.1:n.4740A>C
|
|
|
ENST00000684371.1:n.4773A>C
|
|
|
ENST00000684404.1:n.5695A>C
|
|
|
ENST00000684442.1:n.4891A>C
|
|
|
ENST00000684555.1:c.*2664A>C
|
ENSP00000507705.1:n.*2664A>C
|
|
ENST00000684571.1:c.4293A>C
|
ENSP00000506935.1:p.Gly1431=
|
|
ENST00000684593.1:c.*4157A>C
|
ENSP00000507005.1:n.*4157A>C
|
|
ENST00000684711.1:c.*2848A>C
|
ENSP00000506841.1:n.*2848A>C
|
|
ENST00000302539.9:c.4455A>C
|
ENSP00000303960.4:p.Gly1485=
|
|
ENST00000389817.8:c.4452A>C
MANE Select
|
ENSP00000374467.4:p.Gly1484=
|
|
ENST00000642271.1:c.4449A>C
|
ENSP00000493749.1:p.Gly1483=
|
|
ENST00000642579.1:c.2506A>C
|
|
|
ENST00000642611.1:n.5670A>C
|
|
|
ENST00000642902.1:c.4234A>C
|
|
|
ENST00000643260.1:c.4452A>C
|
ENSP00000494450.1:p.Gly1484=
|
|
ENST00000643562.1:c.*2574A>C
|
ENSP00000496124.1:n.*2574A>C
|
|
ENST00000643925.1:c.3092A>C
|
|
|
ENST00000644057.1:n.611A>C
|
|
|
ENST00000644484.1:c.*3838A>C
|
ENSP00000493558.1:n.*3838A>C
|
|
ENST00000644675.1:c.*2624A>C
|
ENSP00000494567.1:n.*2624A>C
|
|
ENST00000644757.1:c.*3203-1379A>C
|
ENSP00000495085.1:n.*3203-1379A>C
|
|
ENST00000644772.1:c.4518A>C
|
ENSP00000494321.1:p.Gly1506=
|
|
ENST00000645004.1:n.2145A>C
|
|
|
ENST00000645076.1:c.3547A>C
|
|
|
ENST00000645417.1:c.1640A>C
|
|
|
ENST00000645744.1:c.*4137A>C
|
ENSP00000494564.1:n.*4137A>C
|
|
ENST00000645760.1:c.4873A>C
|
|
|
ENST00000645884.1:c.*1735A>C
|
ENSP00000495516.1:n.*1735A>C
|
|
ENST00000646003.1:c.*2474A>C
|
ENSP00000495259.1:n.*2474A>C
|
|
ENST00000646207.1:c.*3289A>C
|
ENSP00000495025.1:n.*3289A>C
|
|
ENST00000646276.1:c.*3856A>C
|
ENSP00000496070.1:n.*3856A>C
|
|
ENST00000646592.1:c.3758A>C
|
|
|
ENST00000646902.1:c.4419A>C
|
ENSP00000494101.1:p.Gly1473=
|
|
ENST00000646993.1:c.*2890A>C
|
ENSP00000493720.1:n.*2890A>C
|
|
ENST00000647013.1:c.4458A>C
|
ENSP00000496741.1:n.4458A>C
|
|
ENST00000647015.1:c.4203A>C
|
ENSP00000495389.1:p.Gly1401=
|
|
ENST00000647086.1:c.*4038A>C
|
ENSP00000493677.1:n.*4038A>C
|
|
ENST00000647158.1:c.*2739A>C
|
ENSP00000495744.1:n.*2739A>C
|
|
ENST00000302539.8:c.4455A>C
|
ENSP00000303960.4:p.Gly1485=
|
|
ENST00000389817.7:c.4452A>C
|
ENSP00000374467.3:p.Gly1484=
|
|
ENST00000525022.1:n.347A>C
|
|
|
ENST00000526037.5:n.212A>C
|
|
|
ENST00000526168.5:c.240A>C
|
|
|
ENST00000531642.5:c.483A>C
|
|
|
NM_000352.4:c.4452A>C
|
NP_000343.2:p.Gly1484=
|
|
NM_001287174.1:c.4455A>C
|
NP_001274103.1:p.Gly1485=
|
|
XM_011520331.1:c.4452A>C
|
XP_011518633.1:p.Gly1484=
|
|
XM_011520332.1:c.4351A>C
|
XP_011518634.1:p.Thr1451Pro
|
|
XM_011520333.1:c.2952A>C
|
XP_011518635.1:p.Gly984=
|
|
XR_930890.1:n.4414A>C
|
|
|
NM_001351295.1:c.4518A>C
|
NP_001338224.1:p.Gly1506=
|
|
NM_001351296.1:c.4452A>C
|
NP_001338225.1:p.Gly1484=
|
|
NM_001351297.1:c.4449A>C
|
NP_001338226.1:p.Gly1483=
|
|
NR_147094.1:n.4747A>C
|
|
|
XM_017018197.2:c.4521A>C
|
XP_016873686.1:p.Gly1507=
|
|
XM_017018199.1:c.4518A>C
|
XP_016873688.1:p.Gly1506=
|
|
XM_017018201.2:c.4417A>C
|
XP_016873690.1:p.Thr1473Pro
|
|
XM_017018202.1:c.3018A>C
|
XP_016873691.1:p.Gly1006=
|
|
XM_017018204.1:c.2409A>C
|
XP_016873693.1:p.Gly803=
|
|
XM_024448668.1:c.2820A>C
|
XP_024304436.1:p.Gly940=
|
|
XR_001747945.2:n.4489A>C
|
|
|
XR_001747946.2:n.4420A>C
|
|
|
XR_002957189.1:n.6203A>C
|
|
|
NM_000352.6:c.4452A>C
MANE Select
|
NP_000343.2:p.Gly1484=
|
|
NM_001287174.2:c.4455A>C
|
NP_001274103.1:p.Gly1485=
|
|
NM_001351295.2:c.4518A>C
|
NP_001338224.1:p.Gly1506=
|
|
NM_001351296.2:c.4452A>C
|
NP_001338225.1:p.Gly1484=
|
|
NM_001351297.2:c.4449A>C
|
NP_001338226.1:p.Gly1483=
|
|
NR_147094.2:n.4747A>C
|
|
|
NM_001287174.3:c.4455A>C
|
NP_001274103.1:p.Gly1485=
|
|