|
ENST00000524561.2:n.4154T>G
|
|
|
|
ENST00000526037.6:n.488T>G
|
|
|
|
ENST00000528374.2:c.1144T>G
|
|
|
|
ENST00000529967.6:n.2892T>G
|
|
|
|
ENST00000532220.2:n.3786T>G
|
|
|
|
ENST00000642611.2:n.5886T>G
|
|
|
|
ENST00000644057.2:n.1129T>G
|
|
|
|
ENST00000645004.2:n.2052T>G
|
|
|
|
ENST00000682051.1:n.4715T>G
|
|
|
|
ENST00000682110.1:n.4768T>G
|
|
|
|
ENST00000682140.1:c.*339T>G
|
ENSP00000507829.1:n.*339T>G
|
|
|
ENST00000682185.1:n.5858T>G
|
|
|
|
ENST00000682204.1:c.*2691T>G
|
ENSP00000507094.1:n.*2691T>G
|
|
|
ENST00000682215.1:n.5135T>G
|
|
|
|
ENST00000682288.1:c.*2984T>G
|
ENSP00000507506.1:n.*2984T>G
|
|
|
ENST00000682442.1:n.4988T>G
|
|
|
|
ENST00000682528.1:n.4845T>G
|
|
|
|
ENST00000682673.1:n.4712T>G
|
|
|
|
ENST00000682805.1:n.5173T>G
|
|
|
|
ENST00000682965.1:c.*975T>G
|
ENSP00000508229.1:n.*975T>G
|
|
|
ENST00000683093.1:n.5748T>G
|
|
|
|
ENST00000683136.1:c.4436T>G
|
ENSP00000507768.1:p.Ile1479Ser
|
|
|
ENST00000683153.1:n.4810T>G
|
|
|
|
ENST00000683365.1:n.4870T>G
|
|
|
|
ENST00000683377.1:n.4664T>G
|
|
|
|
ENST00000683456.1:c.*1690T>G
|
ENSP00000508318.1:n.*1690T>G
|
|
|
ENST00000683522.1:n.4850T>G
|
|
|
|
ENST00000683562.1:c.*2618T>G
|
ENSP00000508265.1:n.*2618T>G
|
|
|
ENST00000683693.1:n.6229T>G
|
|
|
|
ENST00000683725.1:c.*18T>G
|
ENSP00000507496.1:n.*18T>G
|
|
|
ENST00000684010.1:n.4763T>G
|
|
|
|
ENST00000684014.1:n.740T>G
|
|
|
|
ENST00000684157.1:n.5753T>G
|
|
|
|
ENST00000684253.1:n.4671T>G
|
|
|
|
ENST00000684288.1:c.*2725T>G
|
ENSP00000507143.1:n.*2725T>G
|
|
|
ENST00000684313.1:n.4200T>G
|
|
|
|
ENST00000684332.1:n.4841T>G
|
|
|
|
ENST00000684371.1:n.4874T>G
|
|
|
|
ENST00000684404.1:n.5796T>G
|
|
|
|
ENST00000684442.1:n.4992T>G
|
|
|
|
ENST00000684555.1:c.*2765T>G
|
ENSP00000507705.1:n.*2765T>G
|
|
|
ENST00000684571.1:c.4394T>G
|
ENSP00000506935.1:p.Ile1465Ser
|
|
|
ENST00000684593.1:c.*4258T>G
|
ENSP00000507005.1:n.*4258T>G
|
|
|
ENST00000684711.1:c.*2949T>G
|
ENSP00000506841.1:n.*2949T>G
|
|
|
ENST00000302539.9:c.4556T>G
|
ENSP00000303960.4:p.Ile1519Ser
|
|
|
ENST00000389817.8:c.4553T>G
MANE Select
|
ENSP00000374467.4:p.Ile1518Ser
|
|
|
ENST00000642271.1:c.4550T>G
|
ENSP00000493749.1:p.Ile1517Ser
|
|
|
ENST00000642579.1:c.2607T>G
|
|
|
|
ENST00000642611.1:n.5771T>G
|
|
|
|
ENST00000642902.1:c.4335T>G
|
|
|
|
ENST00000643260.1:c.4553T>G
|
ENSP00000494450.1:p.Ile1518Ser
|
|
|
ENST00000643562.1:c.*2675T>G
|
ENSP00000496124.1:n.*2675T>G
|
|
|
ENST00000643925.1:c.3185+514T>G
|
|
|
|
ENST00000644057.1:n.712T>G
|
|
|
|
ENST00000644484.1:c.*3939T>G
|
ENSP00000493558.1:n.*3939T>G
|
|
|
ENST00000644675.1:c.*2725T>G
|
ENSP00000494567.1:n.*2725T>G
|
|
|
ENST00000644757.1:c.*3203-772T>G
|
ENSP00000495085.1:n.*3203-772T>G
|
|
|
ENST00000644772.1:c.4619T>G
|
ENSP00000494321.1:p.Ile1540Ser
|
|
|
ENST00000645004.1:n.2246T>G
|
|
|
|
ENST00000645076.1:c.3648T>G
|
|
|
|
ENST00000645417.1:c.1741T>G
|
|
|
|
ENST00000645744.1:c.*4238T>G
|
ENSP00000494564.1:n.*4238T>G
|
|
|
ENST00000645760.1:c.4974T>G
|
|
|
|
ENST00000645884.1:c.*1836T>G
|
ENSP00000495516.1:n.*1836T>G
|
|
|
ENST00000646003.1:c.*2575T>G
|
ENSP00000495259.1:n.*2575T>G
|
|
|
ENST00000646207.1:c.*3390T>G
|
ENSP00000495025.1:n.*3390T>G
|
|
|
ENST00000646276.1:c.*3957T>G
|
ENSP00000496070.1:n.*3957T>G
|
|
|
ENST00000646592.1:c.3859T>G
|
|
|
|
ENST00000646902.1:c.4520T>G
|
ENSP00000494101.1:p.Ile1507Ser
|
|
|
ENST00000646993.1:c.*2991T>G
|
ENSP00000493720.1:n.*2991T>G
|
|
|
ENST00000647015.1:c.4304T>G
|
ENSP00000495389.1:p.Ile1435Ser
|
|
|
ENST00000647086.1:c.*4139T>G
|
ENSP00000493677.1:n.*4139T>G
|
|
|
ENST00000647158.1:c.*2840T>G
|
ENSP00000495744.1:n.*2840T>G
|
|
|
ENST00000302539.8:c.4556T>G
|
ENSP00000303960.4:p.Ile1519Ser
|
|
|
ENST00000389817.7:c.4553T>G
|
ENSP00000374467.3:p.Ile1518Ser
|
|
|
ENST00000525022.1:n.448T>G
|
|
|
|
ENST00000526037.5:n.313T>G
|
|
|
|
ENST00000526168.5:c.341T>G
|
|
|
|
ENST00000531642.5:c.584T>G
|
|
|
|
NM_000352.4:c.4553T>G
|
NP_000343.2:p.Ile1518Ser
|
|
|
NM_001287174.1:c.4556T>G
|
NP_001274103.1:p.Ile1519Ser
|
|
|
XM_011520331.1:c.4553T>G
|
XP_011518633.1:p.Ile1518Ser
|
|
|
XM_011520333.1:c.3053T>G
|
XP_011518635.1:p.Ile1018Ser
|
|
|
XR_930890.1:n.4515T>G
|
|
|
|
NM_001351295.1:c.4619T>G
|
NP_001338224.1:p.Ile1540Ser
|
|
|
NM_001351296.1:c.4553T>G
|
NP_001338225.1:p.Ile1518Ser
|
|
|
NM_001351297.1:c.4550T>G
|
NP_001338226.1:p.Ile1517Ser
|
|
|
NR_147094.1:n.4848T>G
|
|
|
|
XM_017018197.2:c.4622T>G
|
XP_016873686.1:p.Ile1541Ser
|
|
|
XM_017018199.1:c.4619T>G
|
XP_016873688.1:p.Ile1540Ser
|
|
|
XM_017018202.1:c.3119T>G
|
XP_016873691.1:p.Ile1040Ser
|
|
|
XM_017018204.1:c.2510T>G
|
XP_016873693.1:p.Ile837Ser
|
|
|
XM_024448668.1:c.2921T>G
|
XP_024304436.1:p.Ile974Ser
|
|
|
XR_001747945.2:n.4590T>G
|
|
|
|
XR_001747946.2:n.4521T>G
|
|
|
|
XR_002957189.1:n.6304T>G
|
|
|
|
NM_000352.6:c.4553T>G
MANE Select
|
NP_000343.2:p.Ile1518Ser
|
|
|
NM_001287174.2:c.4556T>G
|
NP_001274103.1:p.Ile1519Ser
|
|
|
NM_001351295.2:c.4619T>G
|
NP_001338224.1:p.Ile1540Ser
|
|
|
NM_001351296.2:c.4553T>G
|
NP_001338225.1:p.Ile1518Ser
|
|
|
NM_001351297.2:c.4550T>G
|
NP_001338226.1:p.Ile1517Ser
|
|
|
NR_147094.2:n.4848T>G
|
|
|
|
NM_001287174.3:c.4556T>G
|
NP_001274103.1:p.Ile1519Ser
|
|
