ENST00000700029.2:c.1102_1103delinsAC
|
ENSP00000514759.2:p.Phe368Thr
|
|
ENST00000710265.1:c.1009_1010delinsAC
|
ENSP00000518161.1:p.Phe337Thr
|
|
ENST00000472832.3:c.1009_1010delinsAC
|
ENSP00000483066.2:p.Phe337Thr
|
|
ENST00000688158.2:n.1744_1745delinsAC
|
|
|
ENST00000688922.2:c.*839_*840delinsAC
|
ENSP00000508742.2:n.*839_*840delinsAC
|
|
ENST00000700021.1:c.964_965delinsAC
|
ENSP00000514757.1:p.Phe322Thr
|
|
ENST00000700022.1:c.*348_*349delinsAC
|
ENSP00000514758.1:n.*348_*349delinsAC
|
|
ENST00000700023.1:n.2167_2168delinsAC
|
|
|
ENST00000700024.1:n.2401_2402delinsAC
|
|
|
ENST00000700025.1:n.1778_1779delinsAC
|
|
|
ENST00000700026.1:n.646_647delinsAC
|
|
|
ENST00000706954.1:c.1009_1010delinsAC
|
ENSP00000516674.1:p.Phe337Thr
|
|
ENST00000706955.1:c.*1044_*1045delinsAC
|
ENSP00000516675.1:n.*1044_*1045delinsAC
|
|
ENST00000686459.1:c.*595_*596delinsAC
|
ENSP00000508909.1:n.*595_*596delinsAC
|
|
ENST00000688158.1:c.*1120_*1121delinsAC
|
ENSP00000509254.1:n.*1120_*1121delinsAC
|
|
ENST00000688308.1:c.1009_1010delinsAC
|
ENSP00000508752.1:p.Phe337Thr
|
|
ENST00000688922.1:c.930_931delinsAC
|
|
|
ENST00000693560.1:c.1528_1529delinsAC
|
ENSP00000509861.1:p.Phe510Thr
|
|
ENST00000371953.8:c.1009_1010delinsAC
MANE Select
|
ENSP00000361021.3:p.Phe337Thr
|
|
ENST00000371953.7:c.1009_1010delinsAC
|
ENSP00000361021.3:p.Phe337Thr
|
|
ENST00000472832.2:c.436_437delinsAC
|
ENSP00000483066.1:p.Phe146Thr
|
|
NM_000314.5:c.1009_1010delinsAC
|
NP_000305.3:p.Phe337Thr
|
|
NM_000314.6:c.1009_1010delinsAC
|
NP_000305.3:p.Phe337Thr
|
|
NM_001304717.2:c.1528_1529delinsAC
|
NP_001291646.2:p.Phe510Thr
|
|
NM_001304718.1:c.418_419delinsAC
|
NP_001291647.1:p.Phe140Thr
|
|
XM_006717926.2:c.964_965delinsAC
|
XP_006717989.1:p.Phe322Thr
|
|
XM_011539981.1:c.1009_1010delinsAC
|
XP_011538283.1:p.Phe337Thr
|
|
XM_011539982.1:c.913_914delinsAC
|
XP_011538284.1:p.Phe305Thr
|
|
XR_945791.1:n.1579_1580delinsAC
|
|
|
NM_000314.7:c.1009_1010delinsAC
|
NP_000305.3:p.Phe337Thr
|
|
NM_001304717.5:c.1528_1529delinsAC
|
NP_001291646.4:p.Phe510Thr
|
|
NM_001304718.2:c.418_419delinsAC
|
NP_001291647.1:p.Phe140Thr
|
|
NM_000314.8:c.1009_1010delinsAC
MANE Select
|
NP_000305.3:p.Phe337Thr
|
|