ENST00000504687.7:c.1173T>G
|
ENSP00000426535.3:p.Ala391=
|
|
ENST00000682650.1:c.1641T>G
|
ENSP00000506904.1:p.Ala547=
|
|
ENST00000683032.1:c.1731T>G
|
ENSP00000506771.1:p.Ala577=
|
|
ENST00000683773.1:n.76T>G
|
|
|
ENST00000684195.1:c.*823T>G
|
ENSP00000508220.1:n.*823T>G
|
|
ENST00000361308.9:c.1731T>G
|
ENSP00000355292.6:p.Ala577=
|
|
ENST00000368300.9:c.1731T>G
MANE Select
|
ENSP00000357283.4:p.Ala577=
|
|
ENST00000496738.6:n.2934T>G
|
|
|
ENST00000674518.1:c.*1081T>G
|
ENSP00000502261.1:n.*1081T>G
|
|
ENST00000674600.1:c.*1530T>G
|
ENSP00000501666.1:n.*1530T>G
|
|
ENST00000674720.1:c.*1037T>G
|
ENSP00000502798.1:n.*1037T>G
|
|
ENST00000675455.1:c.*1531T>G
|
ENSP00000501795.1:n.*1531T>G
|
|
ENST00000675667.1:c.1731T>G
|
ENSP00000501803.1:p.Ala577=
|
|
ENST00000675874.1:c.*1202T>G
|
ENSP00000501851.1:n.*1202T>G
|
|
ENST00000675881.1:c.*742T>G
|
ENSP00000501670.1:n.*742T>G
|
|
ENST00000675939.1:c.1731T>G
|
ENSP00000502256.1:p.Ala577=
|
|
ENST00000675989.1:n.3334T>G
|
|
|
ENST00000676208.1:c.*834T>G
|
ENSP00000502468.1:n.*834T>G
|
|
ENST00000676283.1:n.3271T>G
|
|
|
ENST00000676385.2:c.1641T>G
|
ENSP00000502091.1:p.Ala547=
|
|
ENST00000676434.1:c.*1486T>G
|
ENSP00000501648.1:n.*1486T>G
|
|
ENST00000347559.6:c.1641T>G
|
ENSP00000292304.3:p.Ala547=
|
|
ENST00000368299.7:c.1731T>G
|
ENSP00000357282.3:p.Ala577=
|
|
ENST00000368300.8:c.1731T>G
|
ENSP00000357283.4:p.Ala577=
|
|
ENST00000448611.6:c.1395T>G
|
ENSP00000395597.2:p.Ala465=
|
|
ENST00000473598.6:c.1434T>G
|
ENSP00000421821.1:p.Ala478=
|
|
ENST00000496738.5:n.1944T>G
|
|
|
ENST00000506981.1:n.315T>G
|
|
|
ENST00000508500.1:c.519T>G
|
ENSP00000424977.1:p.Ala173=
|
|
NM_001257374.2:c.1395T>G
|
NP_001244303.1:p.Ala465=
|
|
NM_001282626.1:c.1731T>G
|
NP_001269555.1:p.Ala577=
|
|
NM_170707.3:c.1731T>G
|
NP_733821.1:p.Ala577=
|
|
NM_170708.3:c.1641T>G
|
NP_733822.1:p.Ala547=
|
|
XM_011509533.1:c.1395T>G
|
XP_011507835.1:p.Ala465=
|
|
XM_011509534.1:c.1107T>G
|
XP_011507836.1:p.Ala369=
|
|
XR_921781.1:n.2020T>G
|
|
|
XM_011509534.2:c.1107T>G
|
XP_011507836.1:p.Ala369=
|
|
XR_921781.2:n.2018T>G
|
|
|
NM_170707.4:c.1731T>G
MANE Select
|
NP_733821.1:p.Ala577=
|
|
NM_001257374.3:c.1395T>G
|
NP_001244303.1:p.Ala465=
|
|
NM_001282626.2:c.1731T>G
|
NP_001269555.1:p.Ala577=
|
|
NM_170708.4:c.1641T>G
|
NP_733822.1:p.Ala547=
|
|