|
ENST00000524561.2:n.3664A>G
|
|
|
|
ENST00000528374.2:c.654A>G
|
|
|
|
ENST00000529967.6:n.2402A>G
|
|
|
|
ENST00000532220.2:n.2311A>G
|
|
|
|
ENST00000642611.2:n.4278A>G
|
|
|
|
ENST00000644057.2:n.506A>G
|
|
|
|
ENST00000645004.2:n.1562A>G
|
|
|
|
ENST00000682051.1:n.4225A>G
|
|
|
|
ENST00000682110.1:n.4278A>G
|
|
|
|
ENST00000682140.1:c.3985+221A>G
|
ENSP00000507829.1:n.3985+221A>G
|
|
|
ENST00000682185.1:n.5368A>G
|
|
|
|
ENST00000682204.1:c.*2201A>G
|
ENSP00000507094.1:n.*2201A>G
|
|
|
ENST00000682215.1:n.4645A>G
|
|
|
|
ENST00000682288.1:c.*2494A>G
|
ENSP00000507506.1:n.*2494A>G
|
|
|
ENST00000682442.1:n.4498A>G
|
|
|
|
ENST00000682528.1:n.4355A>G
|
|
|
|
ENST00000682673.1:n.4222A>G
|
|
|
|
ENST00000682805.1:n.4645A>G
|
|
|
|
ENST00000682965.1:c.*485A>G
|
ENSP00000508229.1:n.*485A>G
|
|
|
ENST00000683093.1:n.4377A>G
|
|
|
|
ENST00000683136.1:c.3946A>G
|
ENSP00000507768.1:p.Ser1316Gly
|
|
|
ENST00000683153.1:n.4320A>G
|
|
|
|
ENST00000683365.1:n.4380A>G
|
|
|
|
ENST00000683377.1:n.4278A>G
|
|
|
|
ENST00000683456.1:c.*1200A>G
|
ENSP00000508318.1:n.*1200A>G
|
|
|
ENST00000683522.1:n.4278A>G
|
|
|
|
ENST00000683562.1:c.*2232A>G
|
ENSP00000508265.1:n.*2232A>G
|
|
|
ENST00000683693.1:n.4725A>G
|
|
|
|
ENST00000683725.1:c.4063A>G
|
ENSP00000507496.1:p.Ser1355Gly
|
|
|
ENST00000684010.1:n.4273A>G
|
|
|
|
ENST00000684157.1:n.4278A>G
|
|
|
|
ENST00000684253.1:n.4181A>G
|
|
|
|
ENST00000684288.1:c.*2235A>G
|
ENSP00000507143.1:n.*2235A>G
|
|
|
ENST00000684313.1:n.3710A>G
|
|
|
|
ENST00000684332.1:n.4351A>G
|
|
|
|
ENST00000684371.1:n.4384A>G
|
|
|
|
ENST00000684404.1:n.4321A>G
|
|
|
|
ENST00000684442.1:n.4502A>G
|
|
|
|
ENST00000684555.1:c.*2275A>G
|
ENSP00000507705.1:n.*2275A>G
|
|
|
ENST00000684571.1:c.3904A>G
|
ENSP00000506935.1:p.Ser1302Gly
|
|
|
ENST00000684593.1:c.*3768A>G
|
ENSP00000507005.1:n.*3768A>G
|
|
|
ENST00000684711.1:c.*2459A>G
|
ENSP00000506841.1:n.*2459A>G
|
|
|
ENST00000302539.9:c.4066A>G
|
ENSP00000303960.4:p.Ser1356Gly
|
|
|
ENST00000389817.8:c.4063A>G
MANE Select
|
ENSP00000374467.4:p.Ser1355Gly
|
|
|
ENST00000642271.1:c.4060A>G
|
ENSP00000493749.1:p.Ser1354Gly
|
|
|
ENST00000642579.1:c.2117A>G
|
|
|
|
ENST00000642611.1:n.4163A>G
|
|
|
|
ENST00000642902.1:c.3845A>G
|
|
|
|
ENST00000643260.1:c.4063A>G
|
ENSP00000494450.1:p.Ser1355Gly
|
|
|
ENST00000643562.1:c.*2185A>G
|
ENSP00000496124.1:n.*2185A>G
|
|
|
ENST00000643925.1:c.2703A>G
|
|
|
|
ENST00000644057.1:n.140A>G
|
|
|
|
ENST00000644484.1:c.*2464A>G
|
ENSP00000493558.1:n.*2464A>G
|
|
|
ENST00000644675.1:c.*2235A>G
|
ENSP00000494567.1:n.*2235A>G
|
|
|
ENST00000644757.1:c.*2494A>G
|
ENSP00000495085.1:n.*2494A>G
|
|
|
ENST00000644772.1:c.4129A>G
|
ENSP00000494321.1:p.Ser1377Gly
|
|
|
ENST00000645004.1:n.1718A>G
|
|
|
|
ENST00000645076.1:c.3262A>G
|
|
|
|
ENST00000645417.1:c.1251A>G
|
|
|
|
ENST00000645744.1:c.*2843A>G
|
ENSP00000494564.1:n.*2843A>G
|
|
|
ENST00000645760.1:c.4484A>G
|
|
|
|
ENST00000645884.1:c.*1346A>G
|
ENSP00000495516.1:n.*1346A>G
|
|
|
ENST00000646003.1:c.*2165A>G
|
ENSP00000495259.1:n.*2165A>G
|
|
|
ENST00000646207.1:c.*2900A>G
|
ENSP00000495025.1:n.*2900A>G
|
|
|
ENST00000646276.1:c.*2482A>G
|
ENSP00000496070.1:n.*2482A>G
|
|
|
ENST00000646592.1:c.3369A>G
|
|
|
|
ENST00000646902.1:c.4030A>G
|
ENSP00000494101.1:p.Ser1344Gly
|
|
|
ENST00000646993.1:c.*2605A>G
|
ENSP00000493720.1:n.*2605A>G
|
|
|
ENST00000647013.1:c.4069A>G
|
ENSP00000496741.1:n.4069A>G
|
|
|
ENST00000647015.1:c.3814A>G
|
ENSP00000495389.1:p.Ser1272Gly
|
|
|
ENST00000647086.1:c.*3649A>G
|
ENSP00000493677.1:n.*3649A>G
|
|
|
ENST00000647158.1:c.*2350A>G
|
ENSP00000495744.1:n.*2350A>G
|
|
|
ENST00000302539.8:c.4066A>G
|
ENSP00000303960.4:p.Ser1356Gly
|
|
|
ENST00000389817.7:c.4063A>G
|
ENSP00000374467.3:p.Ser1355Gly
|
|
|
ENST00000527905.5:c.*1085A>G
|
ENSP00000431653.1:n.*1085A>G
|
|
|
ENST00000528374.1:c.545A>G
|
|
|
|
ENST00000531137.1:n.628A>G
|
|
|
|
ENST00000531891.1:c.401A>G
|
|
|
|
ENST00000532220.1:n.537A>G
|
|
|
|
NM_000352.4:c.4063A>G
|
NP_000343.2:p.Ser1355Gly
|
|
|
NM_001287174.1:c.4066A>G
|
NP_001274103.1:p.Ser1356Gly
|
|
|
XM_011520331.1:c.4063A>G
|
XP_011518633.1:p.Ser1355Gly
|
|
|
XM_011520332.1:c.4066A>G
|
XP_011518634.1:p.Ser1356Gly
|
|
|
XM_011520333.1:c.2563A>G
|
XP_011518635.1:p.Ser855Gly
|
|
|
XR_930890.1:n.4129A>G
|
|
|
|
NM_001351295.1:c.4129A>G
|
NP_001338224.1:p.Ser1377Gly
|
|
|
NM_001351296.1:c.4063A>G
|
NP_001338225.1:p.Ser1355Gly
|
|
|
NM_001351297.1:c.4060A>G
|
NP_001338226.1:p.Ser1354Gly
|
|
|
NR_147094.1:n.4358A>G
|
|
|
|
XM_017018197.2:c.4132A>G
|
XP_016873686.1:p.Ser1378Gly
|
|
|
XM_017018199.1:c.4129A>G
|
XP_016873688.1:p.Ser1377Gly
|
|
|
XM_017018201.2:c.4132A>G
|
XP_016873690.1:p.Ser1378Gly
|
|
|
XM_017018202.1:c.2629A>G
|
XP_016873691.1:p.Ser877Gly
|
|
|
XM_017018204.1:c.2020A>G
|
XP_016873693.1:p.Ser674Gly
|
|
|
XM_024448668.1:c.2431A>G
|
XP_024304436.1:p.Ser811Gly
|
|
|
XR_001747945.2:n.4204A>G
|
|
|
|
XR_001747946.2:n.4135A>G
|
|
|
|
XR_002957189.1:n.4800A>G
|
|
|
|
NM_000352.6:c.4063A>G
MANE Select
|
NP_000343.2:p.Ser1355Gly
|
|
|
NM_001287174.2:c.4066A>G
|
NP_001274103.1:p.Ser1356Gly
|
|
|
NM_001351295.2:c.4129A>G
|
NP_001338224.1:p.Ser1377Gly
|
|
|
NM_001351296.2:c.4063A>G
|
NP_001338225.1:p.Ser1355Gly
|
|
|
NM_001351297.2:c.4060A>G
|
NP_001338226.1:p.Ser1354Gly
|
|
|
NR_147094.2:n.4358A>G
|
|
|
|
NM_001287174.3:c.4066A>G
|
NP_001274103.1:p.Ser1356Gly
|
|
