|
ENST00000524561.2:n.4040A>G
|
|
|
|
ENST00000526037.6:n.374A>G
|
|
|
|
ENST00000528374.2:c.1030A>G
|
|
|
|
ENST00000529967.6:n.2778A>G
|
|
|
|
ENST00000532220.2:n.3672A>G
|
|
|
|
ENST00000642611.2:n.5772A>G
|
|
|
|
ENST00000644057.2:n.1015A>G
|
|
|
|
ENST00000645004.2:n.1938A>G
|
|
|
|
ENST00000682051.1:n.4601A>G
|
|
|
|
ENST00000682110.1:n.4654A>G
|
|
|
|
ENST00000682140.1:c.*225A>G
|
ENSP00000507829.1:n.*225A>G
|
|
|
ENST00000682185.1:n.5744A>G
|
|
|
|
ENST00000682204.1:c.*2577A>G
|
ENSP00000507094.1:n.*2577A>G
|
|
|
ENST00000682215.1:n.5021A>G
|
|
|
|
ENST00000682288.1:c.*2870A>G
|
ENSP00000507506.1:n.*2870A>G
|
|
|
ENST00000682442.1:n.4874A>G
|
|
|
|
ENST00000682528.1:n.4731A>G
|
|
|
|
ENST00000682673.1:n.4598A>G
|
|
|
|
ENST00000682805.1:n.5059A>G
|
|
|
|
ENST00000682965.1:c.*861A>G
|
ENSP00000508229.1:n.*861A>G
|
|
|
ENST00000683093.1:n.5634A>G
|
|
|
|
ENST00000683136.1:c.4322A>G
|
ENSP00000507768.1:p.Asn1441Ser
|
|
|
ENST00000683153.1:n.4696A>G
|
|
|
|
ENST00000683365.1:n.4756A>G
|
|
|
|
ENST00000683377.1:n.4550A>G
|
|
|
|
ENST00000683456.1:c.*1576A>G
|
ENSP00000508318.1:n.*1576A>G
|
|
|
ENST00000683522.1:n.4736A>G
|
|
|
|
ENST00000683562.1:c.*2504A>G
|
ENSP00000508265.1:n.*2504A>G
|
|
|
ENST00000683693.1:n.6115A>G
|
|
|
|
ENST00000683725.1:c.4335A>G
|
ENSP00000507496.1:p.Glu1445=
|
|
|
ENST00000684010.1:n.4649A>G
|
|
|
|
ENST00000684014.1:n.626A>G
|
|
|
|
ENST00000684157.1:n.5639A>G
|
|
|
|
ENST00000684253.1:n.4557A>G
|
|
|
|
ENST00000684288.1:c.*2611A>G
|
ENSP00000507143.1:n.*2611A>G
|
|
|
ENST00000684313.1:n.4086A>G
|
|
|
|
ENST00000684332.1:n.4727A>G
|
|
|
|
ENST00000684371.1:n.4760A>G
|
|
|
|
ENST00000684404.1:n.5682A>G
|
|
|
|
ENST00000684442.1:n.4878A>G
|
|
|
|
ENST00000684555.1:c.*2651A>G
|
ENSP00000507705.1:n.*2651A>G
|
|
|
ENST00000684571.1:c.4280A>G
|
ENSP00000506935.1:p.Asn1427Ser
|
|
|
ENST00000684593.1:c.*4144A>G
|
ENSP00000507005.1:n.*4144A>G
|
|
|
ENST00000684711.1:c.*2835A>G
|
ENSP00000506841.1:n.*2835A>G
|
|
|
ENST00000302539.9:c.4442A>G
|
ENSP00000303960.4:p.Asn1481Ser
|
|
|
ENST00000389817.8:c.4439A>G
MANE Select
|
ENSP00000374467.4:p.Asn1480Ser
|
|
|
ENST00000642271.1:c.4436A>G
|
ENSP00000493749.1:p.Asn1479Ser
|
|
|
ENST00000642579.1:c.2493A>G
|
|
|
|
ENST00000642611.1:n.5657A>G
|
|
|
|
ENST00000642902.1:c.4221A>G
|
|
|
|
ENST00000643260.1:c.4439A>G
|
ENSP00000494450.1:p.Asn1480Ser
|
|
|
ENST00000643562.1:c.*2561A>G
|
ENSP00000496124.1:n.*2561A>G
|
|
|
ENST00000643925.1:c.3079A>G
|
|
|
|
ENST00000644057.1:n.598A>G
|
|
|
|
ENST00000644484.1:c.*3825A>G
|
ENSP00000493558.1:n.*3825A>G
|
|
|
ENST00000644675.1:c.*2611A>G
|
ENSP00000494567.1:n.*2611A>G
|
|
|
ENST00000644757.1:c.*3203-1392A>G
|
ENSP00000495085.1:n.*3203-1392A>G
|
|
|
ENST00000644772.1:c.4505A>G
|
ENSP00000494321.1:p.Asn1502Ser
|
|
|
ENST00000645004.1:n.2132A>G
|
|
|
|
ENST00000645076.1:c.3534A>G
|
|
|
|
ENST00000645417.1:c.1627A>G
|
|
|
|
ENST00000645744.1:c.*4124A>G
|
ENSP00000494564.1:n.*4124A>G
|
|
|
ENST00000645760.1:c.4860A>G
|
|
|
|
ENST00000645884.1:c.*1722A>G
|
ENSP00000495516.1:n.*1722A>G
|
|
|
ENST00000646003.1:c.*2461A>G
|
ENSP00000495259.1:n.*2461A>G
|
|
|
ENST00000646207.1:c.*3276A>G
|
ENSP00000495025.1:n.*3276A>G
|
|
|
ENST00000646276.1:c.*3843A>G
|
ENSP00000496070.1:n.*3843A>G
|
|
|
ENST00000646592.1:c.3745A>G
|
|
|
|
ENST00000646902.1:c.4406A>G
|
ENSP00000494101.1:p.Asn1469Ser
|
|
|
ENST00000646993.1:c.*2877A>G
|
ENSP00000493720.1:n.*2877A>G
|
|
|
ENST00000647013.1:c.4445A>G
|
ENSP00000496741.1:n.4445A>G
|
|
|
ENST00000647015.1:c.4190A>G
|
ENSP00000495389.1:p.Asn1397Ser
|
|
|
ENST00000647086.1:c.*4025A>G
|
ENSP00000493677.1:n.*4025A>G
|
|
|
ENST00000647158.1:c.*2726A>G
|
ENSP00000495744.1:n.*2726A>G
|
|
|
ENST00000302539.8:c.4442A>G
|
ENSP00000303960.4:p.Asn1481Ser
|
|
|
ENST00000389817.7:c.4439A>G
|
ENSP00000374467.3:p.Asn1480Ser
|
|
|
ENST00000525022.1:n.334A>G
|
|
|
|
ENST00000526037.5:n.199A>G
|
|
|
|
ENST00000526168.5:c.227A>G
|
|
|
|
ENST00000531642.5:c.470A>G
|
|
|
|
NM_000352.4:c.4439A>G
|
NP_000343.2:p.Asn1480Ser
|
|
|
NM_001287174.1:c.4442A>G
|
NP_001274103.1:p.Asn1481Ser
|
|
|
XM_011520331.1:c.4439A>G
|
XP_011518633.1:p.Asn1480Ser
|
|
|
XM_011520332.1:c.4338A>G
|
XP_011518634.1:p.Glu1446=
|
|
|
XM_011520333.1:c.2939A>G
|
XP_011518635.1:p.Asn980Ser
|
|
|
XR_930890.1:n.4401A>G
|
|
|
|
NM_001351295.1:c.4505A>G
|
NP_001338224.1:p.Asn1502Ser
|
|
|
NM_001351296.1:c.4439A>G
|
NP_001338225.1:p.Asn1480Ser
|
|
|
NM_001351297.1:c.4436A>G
|
NP_001338226.1:p.Asn1479Ser
|
|
|
NR_147094.1:n.4734A>G
|
|
|
|
XM_017018197.2:c.4508A>G
|
XP_016873686.1:p.Asn1503Ser
|
|
|
XM_017018199.1:c.4505A>G
|
XP_016873688.1:p.Asn1502Ser
|
|
|
XM_017018201.2:c.4404A>G
|
XP_016873690.1:p.Glu1468=
|
|
|
XM_017018202.1:c.3005A>G
|
XP_016873691.1:p.Asn1002Ser
|
|
|
XM_017018204.1:c.2396A>G
|
XP_016873693.1:p.Asn799Ser
|
|
|
XM_024448668.1:c.2807A>G
|
XP_024304436.1:p.Asn936Ser
|
|
|
XR_001747945.2:n.4476A>G
|
|
|
|
XR_001747946.2:n.4407A>G
|
|
|
|
XR_002957189.1:n.6190A>G
|
|
|
|
NM_000352.6:c.4439A>G
MANE Select
|
NP_000343.2:p.Asn1480Ser
|
|
|
NM_001287174.2:c.4442A>G
|
NP_001274103.1:p.Asn1481Ser
|
|
|
NM_001351295.2:c.4505A>G
|
NP_001338224.1:p.Asn1502Ser
|
|
|
NM_001351296.2:c.4439A>G
|
NP_001338225.1:p.Asn1480Ser
|
|
|
NM_001351297.2:c.4436A>G
|
NP_001338226.1:p.Asn1479Ser
|
|
|
NR_147094.2:n.4734A>G
|
|
|
|
NM_001287174.3:c.4442A>G
|
NP_001274103.1:p.Asn1481Ser
|
|
