|
ENST00000524561.2:n.4187A>G
|
|
|
|
ENST00000526037.6:n.521A>G
|
|
|
|
ENST00000528374.2:c.1177A>G
|
|
|
|
ENST00000529967.6:n.2925A>G
|
|
|
|
ENST00000532220.2:n.3819A>G
|
|
|
|
ENST00000642611.2:n.5919A>G
|
|
|
|
ENST00000644057.2:n.1162A>G
|
|
|
|
ENST00000645004.2:n.2085A>G
|
|
|
|
ENST00000682051.1:n.4748A>G
|
|
|
|
ENST00000682110.1:n.4801A>G
|
|
|
|
ENST00000682140.1:c.*372A>G
|
ENSP00000507829.1:n.*372A>G
|
|
|
ENST00000682185.1:n.5891A>G
|
|
|
|
ENST00000682204.1:c.*2724A>G
|
ENSP00000507094.1:n.*2724A>G
|
|
|
ENST00000682215.1:n.5168A>G
|
|
|
|
ENST00000682288.1:c.*3017A>G
|
ENSP00000507506.1:n.*3017A>G
|
|
|
ENST00000682442.1:n.5021A>G
|
|
|
|
ENST00000682528.1:n.4878A>G
|
|
|
|
ENST00000682673.1:n.4745A>G
|
|
|
|
ENST00000682805.1:n.5206A>G
|
|
|
|
ENST00000682965.1:c.*1008A>G
|
ENSP00000508229.1:n.*1008A>G
|
|
|
ENST00000683093.1:n.5781A>G
|
|
|
|
ENST00000683136.1:c.4469A>G
|
ENSP00000507768.1:p.Asp1490Gly
|
|
|
ENST00000683153.1:n.4843A>G
|
|
|
|
ENST00000683365.1:n.4903A>G
|
|
|
|
ENST00000683377.1:n.4697A>G
|
|
|
|
ENST00000683456.1:c.*1723A>G
|
ENSP00000508318.1:n.*1723A>G
|
|
|
ENST00000683522.1:n.4883A>G
|
|
|
|
ENST00000683562.1:c.*2651A>G
|
ENSP00000508265.1:n.*2651A>G
|
|
|
ENST00000683693.1:n.6262A>G
|
|
|
|
ENST00000683725.1:c.*51A>G
|
ENSP00000507496.1:n.*51A>G
|
|
|
ENST00000684010.1:n.4796A>G
|
|
|
|
ENST00000684014.1:n.773A>G
|
|
|
|
ENST00000684157.1:n.5786A>G
|
|
|
|
ENST00000684253.1:n.4704A>G
|
|
|
|
ENST00000684288.1:c.*2758A>G
|
ENSP00000507143.1:n.*2758A>G
|
|
|
ENST00000684313.1:n.4233A>G
|
|
|
|
ENST00000684332.1:n.4874A>G
|
|
|
|
ENST00000684371.1:n.4907A>G
|
|
|
|
ENST00000684404.1:n.5829A>G
|
|
|
|
ENST00000684442.1:n.5025A>G
|
|
|
|
ENST00000684555.1:c.*2798A>G
|
ENSP00000507705.1:n.*2798A>G
|
|
|
ENST00000684571.1:c.4427A>G
|
ENSP00000506935.1:p.Asp1476Gly
|
|
|
ENST00000684593.1:c.*4291A>G
|
ENSP00000507005.1:n.*4291A>G
|
|
|
ENST00000684711.1:c.*2982A>G
|
ENSP00000506841.1:n.*2982A>G
|
|
|
ENST00000302539.9:c.4589A>G
|
ENSP00000303960.4:p.Asp1530Gly
|
|
|
ENST00000389817.8:c.4586A>G
MANE Select
|
ENSP00000374467.4:p.Asp1529Gly
|
|
|
ENST00000642271.1:c.4583A>G
|
ENSP00000493749.1:p.Asp1528Gly
|
|
|
ENST00000642579.1:c.2640A>G
|
|
|
|
ENST00000642611.1:n.5804A>G
|
|
|
|
ENST00000642902.1:c.4368A>G
|
|
|
|
ENST00000643260.1:c.4586A>G
|
ENSP00000494450.1:p.Asp1529Gly
|
|
|
ENST00000643562.1:c.*2708A>G
|
ENSP00000496124.1:n.*2708A>G
|
|
|
ENST00000643925.1:c.3185+547A>G
|
|
|
|
ENST00000644057.1:n.745A>G
|
|
|
|
ENST00000644484.1:c.*3972A>G
|
ENSP00000493558.1:n.*3972A>G
|
|
|
ENST00000644675.1:c.*2758A>G
|
ENSP00000494567.1:n.*2758A>G
|
|
|
ENST00000644757.1:c.*3203-739A>G
|
ENSP00000495085.1:n.*3203-739A>G
|
|
|
ENST00000644772.1:c.4652A>G
|
ENSP00000494321.1:p.Asp1551Gly
|
|
|
ENST00000645004.1:n.2279A>G
|
|
|
|
ENST00000645076.1:c.3681A>G
|
|
|
|
ENST00000645417.1:c.1774A>G
|
|
|
|
ENST00000645744.1:c.*4271A>G
|
ENSP00000494564.1:n.*4271A>G
|
|
|
ENST00000645760.1:c.5007A>G
|
|
|
|
ENST00000645884.1:c.*1869A>G
|
ENSP00000495516.1:n.*1869A>G
|
|
|
ENST00000646003.1:c.*2608A>G
|
ENSP00000495259.1:n.*2608A>G
|
|
|
ENST00000646207.1:c.*3423A>G
|
ENSP00000495025.1:n.*3423A>G
|
|
|
ENST00000646276.1:c.*3990A>G
|
ENSP00000496070.1:n.*3990A>G
|
|
|
ENST00000646592.1:c.3892A>G
|
|
|
|
ENST00000646902.1:c.4553A>G
|
ENSP00000494101.1:p.Asp1518Gly
|
|
|
ENST00000646993.1:c.*3024A>G
|
ENSP00000493720.1:n.*3024A>G
|
|
|
ENST00000647015.1:c.4337A>G
|
ENSP00000495389.1:p.Asp1446Gly
|
|
|
ENST00000647086.1:c.*4172A>G
|
ENSP00000493677.1:n.*4172A>G
|
|
|
ENST00000647158.1:c.*2873A>G
|
ENSP00000495744.1:n.*2873A>G
|
|
|
ENST00000302539.8:c.4589A>G
|
ENSP00000303960.4:p.Asp1530Gly
|
|
|
ENST00000389817.7:c.4586A>G
|
ENSP00000374467.3:p.Asp1529Gly
|
|
|
ENST00000525022.1:n.481A>G
|
|
|
|
ENST00000526037.5:n.346A>G
|
|
|
|
ENST00000526168.5:c.374A>G
|
|
|
|
ENST00000531642.5:c.617A>G
|
|
|
|
NM_000352.4:c.4586A>G
|
NP_000343.2:p.Asp1529Gly
|
|
|
NM_001287174.1:c.4589A>G
|
NP_001274103.1:p.Asp1530Gly
|
|
|
XM_011520331.1:c.4586A>G
|
XP_011518633.1:p.Asp1529Gly
|
|
|
XM_011520333.1:c.3086A>G
|
XP_011518635.1:p.Asp1029Gly
|
|
|
XR_930890.1:n.4548A>G
|
|
|
|
NM_001351295.1:c.4652A>G
|
NP_001338224.1:p.Asp1551Gly
|
|
|
NM_001351296.1:c.4586A>G
|
NP_001338225.1:p.Asp1529Gly
|
|
|
NM_001351297.1:c.4583A>G
|
NP_001338226.1:p.Asp1528Gly
|
|
|
NR_147094.1:n.4881A>G
|
|
|
|
XM_017018197.2:c.4655A>G
|
XP_016873686.1:p.Asp1552Gly
|
|
|
XM_017018199.1:c.4652A>G
|
XP_016873688.1:p.Asp1551Gly
|
|
|
XM_017018202.1:c.3152A>G
|
XP_016873691.1:p.Asp1051Gly
|
|
|
XM_017018204.1:c.2543A>G
|
XP_016873693.1:p.Asp848Gly
|
|
|
XM_024448668.1:c.2954A>G
|
XP_024304436.1:p.Asp985Gly
|
|
|
XR_001747945.2:n.4623A>G
|
|
|
|
XR_001747946.2:n.4554A>G
|
|
|
|
XR_002957189.1:n.6337A>G
|
|
|
|
NM_000352.6:c.4586A>G
MANE Select
|
NP_000343.2:p.Asp1529Gly
|
|
|
NM_001287174.2:c.4589A>G
|
NP_001274103.1:p.Asp1530Gly
|
|
|
NM_001351295.2:c.4652A>G
|
NP_001338224.1:p.Asp1551Gly
|
|
|
NM_001351296.2:c.4586A>G
|
NP_001338225.1:p.Asp1529Gly
|
|
|
NM_001351297.2:c.4583A>G
|
NP_001338226.1:p.Asp1528Gly
|
|
|
NR_147094.2:n.4881A>G
|
|
|
|
NM_001287174.3:c.4589A>G
|
NP_001274103.1:p.Asp1530Gly
|
|
