|
ENST00000524561.2:n.4196T>G
|
|
|
|
ENST00000526037.6:n.530T>G
|
|
|
|
ENST00000528374.2:c.1186T>G
|
|
|
|
ENST00000529967.6:n.2934T>G
|
|
|
|
ENST00000532220.2:n.3828T>G
|
|
|
|
ENST00000642611.2:n.5928T>G
|
|
|
|
ENST00000644057.2:n.1171T>G
|
|
|
|
ENST00000645004.2:n.2094T>G
|
|
|
|
ENST00000682051.1:n.4757T>G
|
|
|
|
ENST00000682110.1:n.4810T>G
|
|
|
|
ENST00000682140.1:c.*381T>G
|
ENSP00000507829.1:n.*381T>G
|
|
|
ENST00000682185.1:n.5900T>G
|
|
|
|
ENST00000682204.1:c.*2733T>G
|
ENSP00000507094.1:n.*2733T>G
|
|
|
ENST00000682215.1:n.5177T>G
|
|
|
|
ENST00000682288.1:c.*3026T>G
|
ENSP00000507506.1:n.*3026T>G
|
|
|
ENST00000682442.1:n.5030T>G
|
|
|
|
ENST00000682528.1:n.4887T>G
|
|
|
|
ENST00000682673.1:n.4754T>G
|
|
|
|
ENST00000682805.1:n.5215T>G
|
|
|
|
ENST00000682965.1:c.*1017T>G
|
ENSP00000508229.1:n.*1017T>G
|
|
|
ENST00000683093.1:n.5790T>G
|
|
|
|
ENST00000683136.1:c.4478T>G
|
ENSP00000507768.1:p.Val1493Gly
|
|
|
ENST00000683153.1:n.4852T>G
|
|
|
|
ENST00000683365.1:n.4912T>G
|
|
|
|
ENST00000683377.1:n.4706T>G
|
|
|
|
ENST00000683456.1:c.*1732T>G
|
ENSP00000508318.1:n.*1732T>G
|
|
|
ENST00000683522.1:n.4892T>G
|
|
|
|
ENST00000683562.1:c.*2660T>G
|
ENSP00000508265.1:n.*2660T>G
|
|
|
ENST00000683693.1:n.6271T>G
|
|
|
|
ENST00000683725.1:c.*60T>G
|
ENSP00000507496.1:n.*60T>G
|
|
|
ENST00000684010.1:n.4805T>G
|
|
|
|
ENST00000684014.1:n.782T>G
|
|
|
|
ENST00000684157.1:n.5795T>G
|
|
|
|
ENST00000684253.1:n.4713T>G
|
|
|
|
ENST00000684288.1:c.*2767T>G
|
ENSP00000507143.1:n.*2767T>G
|
|
|
ENST00000684313.1:n.4242T>G
|
|
|
|
ENST00000684332.1:n.4883T>G
|
|
|
|
ENST00000684371.1:n.4916T>G
|
|
|
|
ENST00000684404.1:n.5838T>G
|
|
|
|
ENST00000684442.1:n.5034T>G
|
|
|
|
ENST00000684555.1:c.*2807T>G
|
ENSP00000507705.1:n.*2807T>G
|
|
|
ENST00000684571.1:c.4436T>G
|
ENSP00000506935.1:p.Val1479Gly
|
|
|
ENST00000684593.1:c.*4300T>G
|
ENSP00000507005.1:n.*4300T>G
|
|
|
ENST00000684711.1:c.*2991T>G
|
ENSP00000506841.1:n.*2991T>G
|
|
|
ENST00000302539.9:c.4598T>G
|
ENSP00000303960.4:p.Val1533Gly
|
|
|
ENST00000389817.8:c.4595T>G
MANE Select
|
ENSP00000374467.4:p.Val1532Gly
|
|
|
ENST00000642271.1:c.4592T>G
|
ENSP00000493749.1:p.Val1531Gly
|
|
|
ENST00000642579.1:c.2649T>G
|
|
|
|
ENST00000642611.1:n.5813T>G
|
|
|
|
ENST00000642902.1:c.4377T>G
|
|
|
|
ENST00000643260.1:c.4595T>G
|
ENSP00000494450.1:p.Val1532Gly
|
|
|
ENST00000643562.1:c.*2717T>G
|
ENSP00000496124.1:n.*2717T>G
|
|
|
ENST00000643925.1:c.3185+556T>G
|
|
|
|
ENST00000644057.1:n.754T>G
|
|
|
|
ENST00000644484.1:c.*3981T>G
|
ENSP00000493558.1:n.*3981T>G
|
|
|
ENST00000644675.1:c.*2767T>G
|
ENSP00000494567.1:n.*2767T>G
|
|
|
ENST00000644757.1:c.*3203-730T>G
|
ENSP00000495085.1:n.*3203-730T>G
|
|
|
ENST00000644772.1:c.4661T>G
|
ENSP00000494321.1:p.Val1554Gly
|
|
|
ENST00000645004.1:n.2288T>G
|
|
|
|
ENST00000645076.1:c.3690T>G
|
|
|
|
ENST00000645417.1:c.1783T>G
|
|
|
|
ENST00000645744.1:c.*4280T>G
|
ENSP00000494564.1:n.*4280T>G
|
|
|
ENST00000645760.1:c.5016T>G
|
|
|
|
ENST00000645884.1:c.*1878T>G
|
ENSP00000495516.1:n.*1878T>G
|
|
|
ENST00000646003.1:c.*2617T>G
|
ENSP00000495259.1:n.*2617T>G
|
|
|
ENST00000646207.1:c.*3432T>G
|
ENSP00000495025.1:n.*3432T>G
|
|
|
ENST00000646276.1:c.*3999T>G
|
ENSP00000496070.1:n.*3999T>G
|
|
|
ENST00000646592.1:c.3901T>G
|
|
|
|
ENST00000646902.1:c.4562T>G
|
ENSP00000494101.1:p.Val1521Gly
|
|
|
ENST00000646993.1:c.*3033T>G
|
ENSP00000493720.1:n.*3033T>G
|
|
|
ENST00000647015.1:c.4346T>G
|
ENSP00000495389.1:p.Val1449Gly
|
|
|
ENST00000647086.1:c.*4181T>G
|
ENSP00000493677.1:n.*4181T>G
|
|
|
ENST00000647158.1:c.*2882T>G
|
ENSP00000495744.1:n.*2882T>G
|
|
|
ENST00000302539.8:c.4598T>G
|
ENSP00000303960.4:p.Val1533Gly
|
|
|
ENST00000389817.7:c.4595T>G
|
ENSP00000374467.3:p.Val1532Gly
|
|
|
ENST00000525022.1:n.490T>G
|
|
|
|
ENST00000526037.5:n.355T>G
|
|
|
|
ENST00000526168.5:c.383T>G
|
|
|
|
ENST00000531642.5:c.626T>G
|
|
|
|
NM_000352.4:c.4595T>G
|
NP_000343.2:p.Val1532Gly
|
|
|
NM_001287174.1:c.4598T>G
|
NP_001274103.1:p.Val1533Gly
|
|
|
XM_011520331.1:c.4595T>G
|
XP_011518633.1:p.Val1532Gly
|
|
|
XM_011520333.1:c.3095T>G
|
XP_011518635.1:p.Val1032Gly
|
|
|
XR_930890.1:n.4557T>G
|
|
|
|
NM_001351295.1:c.4661T>G
|
NP_001338224.1:p.Val1554Gly
|
|
|
NM_001351296.1:c.4595T>G
|
NP_001338225.1:p.Val1532Gly
|
|
|
NM_001351297.1:c.4592T>G
|
NP_001338226.1:p.Val1531Gly
|
|
|
NR_147094.1:n.4890T>G
|
|
|
|
XM_017018197.2:c.4664T>G
|
XP_016873686.1:p.Val1555Gly
|
|
|
XM_017018199.1:c.4661T>G
|
XP_016873688.1:p.Val1554Gly
|
|
|
XM_017018202.1:c.3161T>G
|
XP_016873691.1:p.Val1054Gly
|
|
|
XM_017018204.1:c.2552T>G
|
XP_016873693.1:p.Val851Gly
|
|
|
XM_024448668.1:c.2963T>G
|
XP_024304436.1:p.Val988Gly
|
|
|
XR_001747945.2:n.4632T>G
|
|
|
|
XR_001747946.2:n.4563T>G
|
|
|
|
XR_002957189.1:n.6346T>G
|
|
|
|
NM_000352.6:c.4595T>G
MANE Select
|
NP_000343.2:p.Val1532Gly
|
|
|
NM_001287174.2:c.4598T>G
|
NP_001274103.1:p.Val1533Gly
|
|
|
NM_001351295.2:c.4661T>G
|
NP_001338224.1:p.Val1554Gly
|
|
|
NM_001351296.2:c.4595T>G
|
NP_001338225.1:p.Val1532Gly
|
|
|
NM_001351297.2:c.4592T>G
|
NP_001338226.1:p.Val1531Gly
|
|
|
NR_147094.2:n.4890T>G
|
|
|
|
NM_001287174.3:c.4598T>G
|
NP_001274103.1:p.Val1533Gly
|
|
