|
ENST00000700029.2:c.767_768delinsCT
|
ENSP00000514759.2:p.Glu256Ala
|
|
|
ENST00000710265.1:c.767_768delinsCT
|
ENSP00000518161.1:p.Glu256Ala
|
|
|
ENST00000472832.3:c.767_768delinsCT
|
ENSP00000483066.2:p.Glu256Ala
|
|
|
ENST00000688158.2:n.1502_1503delinsCT
|
|
|
|
ENST00000688922.2:c.*597_*598delinsCT
|
ENSP00000508742.2:n.*597_*598delinsCT
|
|
|
ENST00000700021.1:c.722_723delinsCT
|
ENSP00000514757.1:p.Glu241Ala
|
|
|
ENST00000700022.1:c.*106_*107delinsCT
|
ENSP00000514758.1:n.*106_*107delinsCT
|
|
|
ENST00000700023.1:n.1925_1926delinsCT
|
|
|
|
ENST00000700024.1:n.2159_2160delinsCT
|
|
|
|
ENST00000700025.1:n.1536_1537delinsCT
|
|
|
|
ENST00000700026.1:n.404_405delinsCT
|
|
|
|
ENST00000700029.1:c.601_602delinsCT
|
|
|
|
ENST00000706954.1:c.767_768delinsCT
|
ENSP00000516674.1:p.Glu256Ala
|
|
|
ENST00000706955.1:c.*802_*803delinsCT
|
ENSP00000516675.1:n.*802_*803delinsCT
|
|
|
ENST00000686459.1:c.*353_*354delinsCT
|
ENSP00000508909.1:n.*353_*354delinsCT
|
|
|
ENST00000688158.1:c.*878_*879delinsCT
|
ENSP00000509254.1:n.*878_*879delinsCT
|
|
|
ENST00000688308.1:c.767_768delinsCT
|
ENSP00000508752.1:p.Glu256Ala
|
|
|
ENST00000688922.1:c.688_689delinsCT
|
|
|
|
ENST00000693560.1:c.1286_1287delinsCT
|
ENSP00000509861.1:p.Glu429Ala
|
|
|
ENST00000371953.8:c.767_768delinsCT
MANE Select
|
ENSP00000361021.3:p.Glu256Ala
|
|
|
ENST00000371953.7:c.767_768delinsCT
|
ENSP00000361021.3:p.Glu256Ala
|
|
|
ENST00000472832.2:c.194_195delinsCT
|
ENSP00000483066.1:p.Glu65Ala
|
|
|
NM_000314.5:c.767_768delinsCT
|
NP_000305.3:p.Glu256Ala
|
|
|
NM_000314.6:c.767_768delinsCT
|
NP_000305.3:p.Glu256Ala
|
|
|
NM_001304717.2:c.1286_1287delinsCT
|
NP_001291646.2:p.Glu429Ala
|
|
|
NM_001304718.1:c.176_177delinsCT
|
NP_001291647.1:p.Glu59Ala
|
|
|
XM_006717926.2:c.722_723delinsCT
|
XP_006717989.1:p.Glu241Ala
|
|
|
XM_011539981.1:c.767_768delinsCT
|
XP_011538283.1:p.Glu256Ala
|
|
|
XM_011539982.1:c.671_672delinsCT
|
XP_011538284.1:p.Glu224Ala
|
|
|
XR_945791.1:n.1337_1338delinsCT
|
|
|
|
NM_000314.7:c.767_768delinsCT
|
NP_000305.3:p.Glu256Ala
|
|
|
NM_001304717.5:c.1286_1287delinsCT
|
NP_001291646.4:p.Glu429Ala
|
|
|
NM_001304718.2:c.176_177delinsCT
|
NP_001291647.1:p.Glu59Ala
|
|
|
NM_000314.8:c.767_768delinsCT
MANE Select
|
NP_000305.3:p.Glu256Ala
|
|
