ENST00000504687.7:c.159C>T
|
ENSP00000426535.3:p.Ser53=
|
|
ENST00000682650.1:c.717C>T
|
ENSP00000506904.1:p.Ser239=
|
|
ENST00000683032.1:c.717C>T
|
ENSP00000506771.1:p.Ser239=
|
|
ENST00000684195.1:c.717C>T
|
ENSP00000508220.1:p.Ser239=
|
|
ENST00000361308.9:c.717C>T
|
ENSP00000355292.6:p.Ser239=
|
|
ENST00000368300.9:c.717C>T
MANE Select
|
ENSP00000357283.4:p.Ser239=
|
|
ENST00000496738.6:n.1092C>T
|
|
|
ENST00000504687.6:c.53C>T
|
ENSP00000426535.2:p.Ala18Val
|
|
ENST00000674518.1:c.*67C>T
|
ENSP00000502261.1:n.*67C>T
|
|
ENST00000674600.1:c.*516C>T
|
ENSP00000501666.1:n.*516C>T
|
|
ENST00000674720.1:c.717C>T
|
ENSP00000502798.1:p.Ser239=
|
|
ENST00000675431.1:n.410C>T
|
|
|
ENST00000675455.1:c.*517C>T
|
ENSP00000501795.1:n.*517C>T
|
|
ENST00000675667.1:c.717C>T
|
ENSP00000501803.1:p.Ser239=
|
|
ENST00000675874.1:c.*188C>T
|
ENSP00000501851.1:n.*188C>T
|
|
ENST00000675881.1:c.717C>T
|
ENSP00000501670.1:p.Ser239=
|
|
ENST00000675939.1:c.717C>T
|
ENSP00000502256.1:p.Ser239=
|
|
ENST00000675989.1:n.1092C>T
|
|
|
ENST00000676208.1:c.717C>T
|
ENSP00000502468.1:p.Ser239=
|
|
ENST00000676283.1:n.1092C>T
|
|
|
ENST00000676385.2:c.717C>T
|
ENSP00000502091.1:p.Ser239=
|
|
ENST00000676434.1:c.717C>T
|
ENSP00000501648.1:p.Ser239=
|
|
ENST00000677389.1:c.717C>T
MANE Plus Clinical
|
ENSP00000503633.1:p.Ser239=
|
|
ENST00000347559.6:c.717C>T
|
ENSP00000292304.3:p.Ser239=
|
|
ENST00000361308.8:c.717C>T
|
ENSP00000355292.5:p.Ser239=
|
|
ENST00000368297.5:c.474C>T
|
ENSP00000357280.1:p.Ser158=
|
|
ENST00000368299.7:c.717C>T
|
ENSP00000357282.3:p.Ser239=
|
|
ENST00000368300.8:c.717C>T
|
ENSP00000357283.4:p.Ser239=
|
|
ENST00000368301.6:c.717C>T
|
ENSP00000357284.2:p.Ser239=
|
|
ENST00000448611.6:c.381C>T
|
ENSP00000395597.2:p.Ser127=
|
|
ENST00000473598.6:c.420C>T
|
ENSP00000421821.1:p.Ser140=
|
|
ENST00000496738.5:n.62C>T
|
|
|
ENST00000504687.5:c.468C>T
|
ENSP00000426535.1:p.Ser156=
|
|
ENST00000515459.5:c.*391C>T
|
ENSP00000424518.1:n.*391C>T
|
|
ENST00000515824.1:n.78C>T
|
|
|
NM_001257374.2:c.381C>T
|
NP_001244303.1:p.Ser127=
|
|
NM_001282624.1:c.474C>T
|
NP_001269553.1:p.Ser158=
|
|
NM_001282625.1:c.717C>T
|
NP_001269554.1:p.Ser239=
|
|
NM_001282626.1:c.717C>T
|
NP_001269555.1:p.Ser239=
|
|
NM_005572.3:c.717C>T , LRG_254t1:c.717C>T
|
NP_005563.1:p.Ser239=
|
|
NM_170707.3:c.717C>T
|
NP_733821.1:p.Ser239=
|
|
NM_170708.3:c.717C>T
|
NP_733822.1:p.Ser239=
|
|
XM_011509533.1:c.381C>T
|
XP_011507835.1:p.Ser127=
|
|
XM_011509534.1:c.53C>T
|
XP_011507836.1:p.Ala18Val
|
|
XR_921781.1:n.966C>T
|
|
|
XM_011509534.2:c.53C>T
|
XP_011507836.1:p.Ala18Val
|
|
XR_921781.2:n.964C>T
|
|
|
NM_170707.4:c.717C>T
MANE Select
|
NP_733821.1:p.Ser239=
|
|
NM_001257374.3:c.381C>T
|
NP_001244303.1:p.Ser127=
|
|
NM_001282626.2:c.717C>T
|
NP_001269555.1:p.Ser239=
|
|
NM_001282624.2:c.474C>T
|
NP_001269553.1:p.Ser158=
|
|
NM_001282625.2:c.717C>T
|
NP_001269554.1:p.Ser239=
|
|
NM_005572.4:c.717C>T
MANE Plus Clinical
|
NP_005563.1:p.Ser239=
|
|
NM_170708.4:c.717C>T
|
NP_733822.1:p.Ser239=
|
|