|
ENST00000524561.2:n.4199T>G
|
|
|
|
ENST00000526037.6:n.533T>G
|
|
|
|
ENST00000528374.2:c.1189T>G
|
|
|
|
ENST00000529967.6:n.2937T>G
|
|
|
|
ENST00000532220.2:n.3831T>G
|
|
|
|
ENST00000642611.2:n.5931T>G
|
|
|
|
ENST00000644057.2:n.1174T>G
|
|
|
|
ENST00000645004.2:n.2097T>G
|
|
|
|
ENST00000682051.1:n.4760T>G
|
|
|
|
ENST00000682110.1:n.4813T>G
|
|
|
|
ENST00000682140.1:c.*384T>G
|
ENSP00000507829.1:n.*384T>G
|
|
|
ENST00000682185.1:n.5903T>G
|
|
|
|
ENST00000682204.1:c.*2736T>G
|
ENSP00000507094.1:n.*2736T>G
|
|
|
ENST00000682215.1:n.5180T>G
|
|
|
|
ENST00000682288.1:c.*3029T>G
|
ENSP00000507506.1:n.*3029T>G
|
|
|
ENST00000682442.1:n.5033T>G
|
|
|
|
ENST00000682528.1:n.4890T>G
|
|
|
|
ENST00000682673.1:n.4757T>G
|
|
|
|
ENST00000682805.1:n.5218T>G
|
|
|
|
ENST00000682965.1:c.*1020T>G
|
ENSP00000508229.1:n.*1020T>G
|
|
|
ENST00000683093.1:n.5793T>G
|
|
|
|
ENST00000683136.1:c.4481T>G
|
ENSP00000507768.1:p.Val1494Gly
|
|
|
ENST00000683153.1:n.4855T>G
|
|
|
|
ENST00000683365.1:n.4915T>G
|
|
|
|
ENST00000683377.1:n.4709T>G
|
|
|
|
ENST00000683456.1:c.*1735T>G
|
ENSP00000508318.1:n.*1735T>G
|
|
|
ENST00000683522.1:n.4895T>G
|
|
|
|
ENST00000683562.1:c.*2663T>G
|
ENSP00000508265.1:n.*2663T>G
|
|
|
ENST00000683693.1:n.6274T>G
|
|
|
|
ENST00000683725.1:c.*63T>G
|
ENSP00000507496.1:n.*63T>G
|
|
|
ENST00000684010.1:n.4808T>G
|
|
|
|
ENST00000684014.1:n.785T>G
|
|
|
|
ENST00000684157.1:n.5798T>G
|
|
|
|
ENST00000684253.1:n.4716T>G
|
|
|
|
ENST00000684288.1:c.*2770T>G
|
ENSP00000507143.1:n.*2770T>G
|
|
|
ENST00000684313.1:n.4245T>G
|
|
|
|
ENST00000684332.1:n.4886T>G
|
|
|
|
ENST00000684371.1:n.4919T>G
|
|
|
|
ENST00000684404.1:n.5841T>G
|
|
|
|
ENST00000684442.1:n.5037T>G
|
|
|
|
ENST00000684555.1:c.*2810T>G
|
ENSP00000507705.1:n.*2810T>G
|
|
|
ENST00000684571.1:c.4439T>G
|
ENSP00000506935.1:p.Val1480Gly
|
|
|
ENST00000684593.1:c.*4303T>G
|
ENSP00000507005.1:n.*4303T>G
|
|
|
ENST00000684711.1:c.*2994T>G
|
ENSP00000506841.1:n.*2994T>G
|
|
|
ENST00000302539.9:c.4601T>G
|
ENSP00000303960.4:p.Val1534Gly
|
|
|
ENST00000389817.8:c.4598T>G
MANE Select
|
ENSP00000374467.4:p.Val1533Gly
|
|
|
ENST00000642271.1:c.4595T>G
|
ENSP00000493749.1:p.Val1532Gly
|
|
|
ENST00000642579.1:c.2652T>G
|
|
|
|
ENST00000642611.1:n.5816T>G
|
|
|
|
ENST00000642902.1:c.4380T>G
|
|
|
|
ENST00000643260.1:c.4598T>G
|
ENSP00000494450.1:p.Val1533Gly
|
|
|
ENST00000643562.1:c.*2720T>G
|
ENSP00000496124.1:n.*2720T>G
|
|
|
ENST00000643925.1:c.3185+559T>G
|
|
|
|
ENST00000644057.1:n.757T>G
|
|
|
|
ENST00000644484.1:c.*3984T>G
|
ENSP00000493558.1:n.*3984T>G
|
|
|
ENST00000644675.1:c.*2770T>G
|
ENSP00000494567.1:n.*2770T>G
|
|
|
ENST00000644757.1:c.*3203-727T>G
|
ENSP00000495085.1:n.*3203-727T>G
|
|
|
ENST00000644772.1:c.4664T>G
|
ENSP00000494321.1:p.Val1555Gly
|
|
|
ENST00000645004.1:n.2291T>G
|
|
|
|
ENST00000645076.1:c.3693T>G
|
|
|
|
ENST00000645417.1:c.1786T>G
|
|
|
|
ENST00000645744.1:c.*4283T>G
|
ENSP00000494564.1:n.*4283T>G
|
|
|
ENST00000645760.1:c.5019T>G
|
|
|
|
ENST00000645884.1:c.*1881T>G
|
ENSP00000495516.1:n.*1881T>G
|
|
|
ENST00000646003.1:c.*2620T>G
|
ENSP00000495259.1:n.*2620T>G
|
|
|
ENST00000646207.1:c.*3435T>G
|
ENSP00000495025.1:n.*3435T>G
|
|
|
ENST00000646276.1:c.*4002T>G
|
ENSP00000496070.1:n.*4002T>G
|
|
|
ENST00000646592.1:c.3904T>G
|
|
|
|
ENST00000646902.1:c.4565T>G
|
ENSP00000494101.1:p.Val1522Gly
|
|
|
ENST00000646993.1:c.*3036T>G
|
ENSP00000493720.1:n.*3036T>G
|
|
|
ENST00000647015.1:c.4349T>G
|
ENSP00000495389.1:p.Val1450Gly
|
|
|
ENST00000647086.1:c.*4184T>G
|
ENSP00000493677.1:n.*4184T>G
|
|
|
ENST00000647158.1:c.*2885T>G
|
ENSP00000495744.1:n.*2885T>G
|
|
|
ENST00000302539.8:c.4601T>G
|
ENSP00000303960.4:p.Val1534Gly
|
|
|
ENST00000389817.7:c.4598T>G
|
ENSP00000374467.3:p.Val1533Gly
|
|
|
ENST00000525022.1:n.493T>G
|
|
|
|
ENST00000526037.5:n.358T>G
|
|
|
|
ENST00000526168.5:c.386T>G
|
|
|
|
ENST00000531642.5:c.629T>G
|
|
|
|
NM_000352.4:c.4598T>G
|
NP_000343.2:p.Val1533Gly
|
|
|
NM_001287174.1:c.4601T>G
|
NP_001274103.1:p.Val1534Gly
|
|
|
XM_011520331.1:c.4598T>G
|
XP_011518633.1:p.Val1533Gly
|
|
|
XM_011520333.1:c.3098T>G
|
XP_011518635.1:p.Val1033Gly
|
|
|
XR_930890.1:n.4560T>G
|
|
|
|
NM_001351295.1:c.4664T>G
|
NP_001338224.1:p.Val1555Gly
|
|
|
NM_001351296.1:c.4598T>G
|
NP_001338225.1:p.Val1533Gly
|
|
|
NM_001351297.1:c.4595T>G
|
NP_001338226.1:p.Val1532Gly
|
|
|
NR_147094.1:n.4893T>G
|
|
|
|
XM_017018197.2:c.4667T>G
|
XP_016873686.1:p.Val1556Gly
|
|
|
XM_017018199.1:c.4664T>G
|
XP_016873688.1:p.Val1555Gly
|
|
|
XM_017018202.1:c.3164T>G
|
XP_016873691.1:p.Val1055Gly
|
|
|
XM_017018204.1:c.2555T>G
|
XP_016873693.1:p.Val852Gly
|
|
|
XM_024448668.1:c.2966T>G
|
XP_024304436.1:p.Val989Gly
|
|
|
XR_001747945.2:n.4635T>G
|
|
|
|
XR_001747946.2:n.4566T>G
|
|
|
|
XR_002957189.1:n.6349T>G
|
|
|
|
NM_000352.6:c.4598T>G
MANE Select
|
NP_000343.2:p.Val1533Gly
|
|
|
NM_001287174.2:c.4601T>G
|
NP_001274103.1:p.Val1534Gly
|
|
|
NM_001351295.2:c.4664T>G
|
NP_001338224.1:p.Val1555Gly
|
|
|
NM_001351296.2:c.4598T>G
|
NP_001338225.1:p.Val1533Gly
|
|
|
NM_001351297.2:c.4595T>G
|
NP_001338226.1:p.Val1532Gly
|
|
|
NR_147094.2:n.4893T>G
|
|
|
|
NM_001287174.3:c.4601T>G
|
NP_001274103.1:p.Val1534Gly
|
|
