ENST00000524561.2:n.4046G>C
|
|
|
ENST00000526037.6:n.380G>C
|
|
|
ENST00000528374.2:c.1036G>C
|
|
|
ENST00000529967.6:n.2784G>C
|
|
|
ENST00000532220.2:n.3678G>C
|
|
|
ENST00000642611.2:n.5778G>C
|
|
|
ENST00000644057.2:n.1021G>C
|
|
|
ENST00000645004.2:n.1944G>C
|
|
|
ENST00000682051.1:n.4607G>C
|
|
|
ENST00000682110.1:n.4660G>C
|
|
|
ENST00000682140.1:c.*231G>C
|
ENSP00000507829.1:n.*231G>C
|
|
ENST00000682185.1:n.5750G>C
|
|
|
ENST00000682204.1:c.*2583G>C
|
ENSP00000507094.1:n.*2583G>C
|
|
ENST00000682215.1:n.5027G>C
|
|
|
ENST00000682288.1:c.*2876G>C
|
ENSP00000507506.1:n.*2876G>C
|
|
ENST00000682442.1:n.4880G>C
|
|
|
ENST00000682528.1:n.4737G>C
|
|
|
ENST00000682673.1:n.4604G>C
|
|
|
ENST00000682805.1:n.5065G>C
|
|
|
ENST00000682965.1:c.*867G>C
|
ENSP00000508229.1:n.*867G>C
|
|
ENST00000683093.1:n.5640G>C
|
|
|
ENST00000683136.1:c.4328G>C
|
ENSP00000507768.1:p.Ser1443Thr
|
|
ENST00000683153.1:n.4702G>C
|
|
|
ENST00000683365.1:n.4762G>C
|
|
|
ENST00000683377.1:n.4556G>C
|
|
|
ENST00000683456.1:c.*1582G>C
|
ENSP00000508318.1:n.*1582G>C
|
|
ENST00000683522.1:n.4742G>C
|
|
|
ENST00000683562.1:c.*2510G>C
|
ENSP00000508265.1:n.*2510G>C
|
|
ENST00000683693.1:n.6121G>C
|
|
|
ENST00000683725.1:c.4341G>C
|
ENSP00000507496.1:p.Gln1447His
|
|
ENST00000684010.1:n.4655G>C
|
|
|
ENST00000684014.1:n.632G>C
|
|
|
ENST00000684157.1:n.5645G>C
|
|
|
ENST00000684253.1:n.4563G>C
|
|
|
ENST00000684288.1:c.*2617G>C
|
ENSP00000507143.1:n.*2617G>C
|
|
ENST00000684313.1:n.4092G>C
|
|
|
ENST00000684332.1:n.4733G>C
|
|
|
ENST00000684371.1:n.4766G>C
|
|
|
ENST00000684404.1:n.5688G>C
|
|
|
ENST00000684442.1:n.4884G>C
|
|
|
ENST00000684555.1:c.*2657G>C
|
ENSP00000507705.1:n.*2657G>C
|
|
ENST00000684571.1:c.4286G>C
|
ENSP00000506935.1:p.Ser1429Thr
|
|
ENST00000684593.1:c.*4150G>C
|
ENSP00000507005.1:n.*4150G>C
|
|
ENST00000684711.1:c.*2841G>C
|
ENSP00000506841.1:n.*2841G>C
|
|
ENST00000302539.9:c.4448G>C
|
ENSP00000303960.4:p.Ser1483Thr
|
|
ENST00000389817.8:c.4445G>C
MANE Select
|
ENSP00000374467.4:p.Ser1482Thr
|
|
ENST00000642271.1:c.4442G>C
|
ENSP00000493749.1:p.Ser1481Thr
|
|
ENST00000642579.1:c.2499G>C
|
|
|
ENST00000642611.1:n.5663G>C
|
|
|
ENST00000642902.1:c.4227G>C
|
|
|
ENST00000643260.1:c.4445G>C
|
ENSP00000494450.1:p.Ser1482Thr
|
|
ENST00000643562.1:c.*2567G>C
|
ENSP00000496124.1:n.*2567G>C
|
|
ENST00000643925.1:c.3085G>C
|
|
|
ENST00000644057.1:n.604G>C
|
|
|
ENST00000644484.1:c.*3831G>C
|
ENSP00000493558.1:n.*3831G>C
|
|
ENST00000644675.1:c.*2617G>C
|
ENSP00000494567.1:n.*2617G>C
|
|
ENST00000644757.1:c.*3203-1386G>C
|
ENSP00000495085.1:n.*3203-1386G>C
|
|
ENST00000644772.1:c.4511G>C
|
ENSP00000494321.1:p.Ser1504Thr
|
|
ENST00000645004.1:n.2138G>C
|
|
|
ENST00000645076.1:c.3540G>C
|
|
|
ENST00000645417.1:c.1633G>C
|
|
|
ENST00000645744.1:c.*4130G>C
|
ENSP00000494564.1:n.*4130G>C
|
|
ENST00000645760.1:c.4866G>C
|
|
|
ENST00000645884.1:c.*1728G>C
|
ENSP00000495516.1:n.*1728G>C
|
|
ENST00000646003.1:c.*2467G>C
|
ENSP00000495259.1:n.*2467G>C
|
|
ENST00000646207.1:c.*3282G>C
|
ENSP00000495025.1:n.*3282G>C
|
|
ENST00000646276.1:c.*3849G>C
|
ENSP00000496070.1:n.*3849G>C
|
|
ENST00000646592.1:c.3751G>C
|
|
|
ENST00000646902.1:c.4412G>C
|
ENSP00000494101.1:p.Ser1471Thr
|
|
ENST00000646993.1:c.*2883G>C
|
ENSP00000493720.1:n.*2883G>C
|
|
ENST00000647013.1:c.4451G>C
|
ENSP00000496741.1:n.4451G>C
|
|
ENST00000647015.1:c.4196G>C
|
ENSP00000495389.1:p.Ser1399Thr
|
|
ENST00000647086.1:c.*4031G>C
|
ENSP00000493677.1:n.*4031G>C
|
|
ENST00000647158.1:c.*2732G>C
|
ENSP00000495744.1:n.*2732G>C
|
|
ENST00000302539.8:c.4448G>C
|
ENSP00000303960.4:p.Ser1483Thr
|
|
ENST00000389817.7:c.4445G>C
|
ENSP00000374467.3:p.Ser1482Thr
|
|
ENST00000525022.1:n.340G>C
|
|
|
ENST00000526037.5:n.205G>C
|
|
|
ENST00000526168.5:c.233G>C
|
|
|
ENST00000531642.5:c.476G>C
|
|
|
NM_000352.4:c.4445G>C
|
NP_000343.2:p.Ser1482Thr
|
|
NM_001287174.1:c.4448G>C
|
NP_001274103.1:p.Ser1483Thr
|
|
XM_011520331.1:c.4445G>C
|
XP_011518633.1:p.Ser1482Thr
|
|
XM_011520332.1:c.4344G>C
|
XP_011518634.1:p.Gln1448His
|
|
XM_011520333.1:c.2945G>C
|
XP_011518635.1:p.Ser982Thr
|
|
XR_930890.1:n.4407G>C
|
|
|
NM_001351295.1:c.4511G>C
|
NP_001338224.1:p.Ser1504Thr
|
|
NM_001351296.1:c.4445G>C
|
NP_001338225.1:p.Ser1482Thr
|
|
NM_001351297.1:c.4442G>C
|
NP_001338226.1:p.Ser1481Thr
|
|
NR_147094.1:n.4740G>C
|
|
|
XM_017018197.2:c.4514G>C
|
XP_016873686.1:p.Ser1505Thr
|
|
XM_017018199.1:c.4511G>C
|
XP_016873688.1:p.Ser1504Thr
|
|
XM_017018201.2:c.4410G>C
|
XP_016873690.1:p.Gln1470His
|
|
XM_017018202.1:c.3011G>C
|
XP_016873691.1:p.Ser1004Thr
|
|
XM_017018204.1:c.2402G>C
|
XP_016873693.1:p.Ser801Thr
|
|
XM_024448668.1:c.2813G>C
|
XP_024304436.1:p.Ser938Thr
|
|
XR_001747945.2:n.4482G>C
|
|
|
XR_001747946.2:n.4413G>C
|
|
|
XR_002957189.1:n.6196G>C
|
|
|
NM_000352.6:c.4445G>C
MANE Select
|
NP_000343.2:p.Ser1482Thr
|
|
NM_001287174.2:c.4448G>C
|
NP_001274103.1:p.Ser1483Thr
|
|
NM_001351295.2:c.4511G>C
|
NP_001338224.1:p.Ser1504Thr
|
|
NM_001351296.2:c.4445G>C
|
NP_001338225.1:p.Ser1482Thr
|
|
NM_001351297.2:c.4442G>C
|
NP_001338226.1:p.Ser1481Thr
|
|
NR_147094.2:n.4740G>C
|
|
|
NM_001287174.3:c.4448G>C
|
NP_001274103.1:p.Ser1483Thr
|
|