ENST00000700029.2:c.743_744delinsCT
|
ENSP00000514759.2:p.Pro248=
|
|
ENST00000710265.1:c.743_744delinsCT
|
ENSP00000518161.1:p.Pro248=
|
|
ENST00000472832.3:c.743_744delinsCT
|
ENSP00000483066.2:p.Pro248=
|
|
ENST00000688158.2:n.1478_1479delinsCT
|
|
|
ENST00000688922.2:c.*573_*574delinsCT
|
ENSP00000508742.2:n.*573_*574delinsCT
|
|
ENST00000700021.1:c.698_699delinsCT
|
ENSP00000514757.1:p.Pro233=
|
|
ENST00000700022.1:c.*82_*83delinsCT
|
ENSP00000514758.1:n.*82_*83delinsCT
|
|
ENST00000700023.1:n.1901_1902delinsCT
|
|
|
ENST00000700024.1:n.2135_2136delinsCT
|
|
|
ENST00000700025.1:n.1512_1513delinsCT
|
|
|
ENST00000700026.1:n.380_381delinsCT
|
|
|
ENST00000700029.1:c.577_578delinsCT
|
|
|
ENST00000706954.1:c.743_744delinsCT
|
ENSP00000516674.1:p.Pro248=
|
|
ENST00000706955.1:c.*778_*779delinsCT
|
ENSP00000516675.1:n.*778_*779delinsCT
|
|
ENST00000686459.1:c.*329_*330delinsCT
|
ENSP00000508909.1:n.*329_*330delinsCT
|
|
ENST00000688158.1:c.*854_*855delinsCT
|
ENSP00000509254.1:n.*854_*855delinsCT
|
|
ENST00000688308.1:c.743_744delinsCT
|
ENSP00000508752.1:p.Pro248=
|
|
ENST00000688922.1:c.664_665delinsCT
|
|
|
ENST00000693560.1:c.1262_1263delinsCT
|
ENSP00000509861.1:p.Pro421=
|
|
ENST00000371953.8:c.743_744delinsCT
MANE Select
|
ENSP00000361021.3:p.Pro248=
|
|
ENST00000371953.7:c.743_744delinsCT
|
ENSP00000361021.3:p.Pro248=
|
|
ENST00000472832.2:c.170_171delinsCT
|
ENSP00000483066.1:p.Pro57=
|
|
NM_000314.5:c.743_744delinsCT
|
NP_000305.3:p.Pro248=
|
|
NM_000314.6:c.743_744delinsCT
|
NP_000305.3:p.Pro248=
|
|
NM_001304717.2:c.1262_1263delinsCT
|
NP_001291646.2:p.Pro421=
|
|
NM_001304718.1:c.152_153delinsCT
|
NP_001291647.1:p.Pro51=
|
|
XM_006717926.2:c.698_699delinsCT
|
XP_006717989.1:p.Pro233=
|
|
XM_011539981.1:c.743_744delinsCT
|
XP_011538283.1:p.Pro248=
|
|
XM_011539982.1:c.647_648delinsCT
|
XP_011538284.1:p.Pro216=
|
|
XR_945791.1:n.1313_1314delinsCT
|
|
|
NM_000314.7:c.743_744delinsCT
|
NP_000305.3:p.Pro248=
|
|
NM_001304717.5:c.1262_1263delinsCT
|
NP_001291646.4:p.Pro421=
|
|
NM_001304718.2:c.152_153delinsCT
|
NP_001291647.1:p.Pro51=
|
|
NM_000314.8:c.743_744delinsCT
MANE Select
|
NP_000305.3:p.Pro248=
|
|