|
ENST00000700029.2:c.766_767delinsAC
|
ENSP00000514759.2:p.Glu256Thr
|
|
|
ENST00000710265.1:c.766_767delinsAC
|
ENSP00000518161.1:p.Glu256Thr
|
|
|
ENST00000472832.3:c.766_767delinsAC
|
ENSP00000483066.2:p.Glu256Thr
|
|
|
ENST00000688158.2:n.1501_1502delinsAC
|
|
|
|
ENST00000688922.2:c.*596_*597delinsAC
|
ENSP00000508742.2:n.*596_*597delinsAC
|
|
|
ENST00000700021.1:c.721_722delinsAC
|
ENSP00000514757.1:p.Glu241Thr
|
|
|
ENST00000700022.1:c.*105_*106delinsAC
|
ENSP00000514758.1:n.*105_*106delinsAC
|
|
|
ENST00000700023.1:n.1924_1925delinsAC
|
|
|
|
ENST00000700024.1:n.2158_2159delinsAC
|
|
|
|
ENST00000700025.1:n.1535_1536delinsAC
|
|
|
|
ENST00000700026.1:n.403_404delinsAC
|
|
|
|
ENST00000700029.1:c.600_601delinsAC
|
|
|
|
ENST00000706954.1:c.766_767delinsAC
|
ENSP00000516674.1:p.Glu256Thr
|
|
|
ENST00000706955.1:c.*801_*802delinsAC
|
ENSP00000516675.1:n.*801_*802delinsAC
|
|
|
ENST00000686459.1:c.*352_*353delinsAC
|
ENSP00000508909.1:n.*352_*353delinsAC
|
|
|
ENST00000688158.1:c.*877_*878delinsAC
|
ENSP00000509254.1:n.*877_*878delinsAC
|
|
|
ENST00000688308.1:c.766_767delinsAC
|
ENSP00000508752.1:p.Glu256Thr
|
|
|
ENST00000688922.1:c.687_688delinsAC
|
|
|
|
ENST00000693560.1:c.1285_1286delinsAC
|
ENSP00000509861.1:p.Glu429Thr
|
|
|
ENST00000371953.8:c.766_767delinsAC
MANE Select
|
ENSP00000361021.3:p.Glu256Thr
|
|
|
ENST00000371953.7:c.766_767delinsAC
|
ENSP00000361021.3:p.Glu256Thr
|
|
|
ENST00000472832.2:c.193_194delinsAC
|
ENSP00000483066.1:p.Glu65Thr
|
|
|
NM_000314.5:c.766_767delinsAC
|
NP_000305.3:p.Glu256Thr
|
|
|
NM_000314.6:c.766_767delinsAC
|
NP_000305.3:p.Glu256Thr
|
|
|
NM_001304717.2:c.1285_1286delinsAC
|
NP_001291646.2:p.Glu429Thr
|
|
|
NM_001304718.1:c.175_176delinsAC
|
NP_001291647.1:p.Glu59Thr
|
|
|
XM_006717926.2:c.721_722delinsAC
|
XP_006717989.1:p.Glu241Thr
|
|
|
XM_011539981.1:c.766_767delinsAC
|
XP_011538283.1:p.Glu256Thr
|
|
|
XM_011539982.1:c.670_671delinsAC
|
XP_011538284.1:p.Glu224Thr
|
|
|
XR_945791.1:n.1336_1337delinsAC
|
|
|
|
NM_000314.7:c.766_767delinsAC
|
NP_000305.3:p.Glu256Thr
|
|
|
NM_001304717.5:c.1285_1286delinsAC
|
NP_001291646.4:p.Glu429Thr
|
|
|
NM_001304718.2:c.175_176delinsAC
|
NP_001291647.1:p.Glu59Thr
|
|
|
NM_000314.8:c.766_767delinsAC
MANE Select
|
NP_000305.3:p.Glu256Thr
|
|
