ENST00000700029.2:c.756_757insC
|
ENSP00000514759.2:p.Ile253HisfsTer?
|
|
ENST00000710265.1:c.756_757insC
|
ENSP00000518161.1:p.Ile253HisfsTer?
|
|
ENST00000472832.3:c.756_757insC
|
ENSP00000483066.2:p.Ile253HisfsTer?
|
|
ENST00000688158.2:n.1491_1492insC
|
|
|
ENST00000688922.2:c.*586_*587insC
|
ENSP00000508742.2:n.*586_*587insC
|
|
ENST00000700021.1:c.711_712insC
|
ENSP00000514757.1:p.Ile238HisfsTer?
|
|
ENST00000700022.1:c.*95_*96insC
|
ENSP00000514758.1:n.*95_*96insC
|
|
ENST00000700023.1:n.1914_1915insC
|
|
|
ENST00000700024.1:n.2148_2149insC
|
|
|
ENST00000700025.1:n.1525_1526insC
|
|
|
ENST00000700026.1:n.393_394insC
|
|
|
ENST00000700029.1:c.590_591insC
|
|
|
ENST00000706954.1:c.756_757insC
|
ENSP00000516674.1:p.Ile253HisfsTer?
|
|
ENST00000706955.1:c.*791_*792insC
|
ENSP00000516675.1:n.*791_*792insC
|
|
ENST00000686459.1:c.*342_*343insC
|
ENSP00000508909.1:n.*342_*343insC
|
|
ENST00000688158.1:c.*867_*868insC
|
ENSP00000509254.1:n.*867_*868insC
|
|
ENST00000688308.1:c.756_757insC
|
ENSP00000508752.1:p.Ile253HisfsTer?
|
|
ENST00000688922.1:c.677_678insC
|
|
|
ENST00000693560.1:c.1275_1276insC
|
ENSP00000509861.1:p.Ile426HisfsTer?
|
|
ENST00000371953.8:c.756_757insC
MANE Select
|
ENSP00000361021.3:p.Ile253HisfsTer?
|
|
ENST00000371953.7:c.756_757insC
|
ENSP00000361021.3:p.Ile253HisfsTer?
|
|
ENST00000472832.2:c.183_184insC
|
ENSP00000483066.1:p.Ile62HisfsTer?
|
|
NM_000314.5:c.756_757insC
|
NP_000305.3:p.Ile253HisfsTer?
|
|
NM_000314.6:c.756_757insC
|
NP_000305.3:p.Ile253HisfsTer?
|
|
NM_001304717.2:c.1275_1276insC
|
NP_001291646.2:p.Ile426HisfsTer?
|
|
NM_001304718.1:c.165_166insC
|
NP_001291647.1:p.Ile56HisfsTer?
|
|
XM_006717926.2:c.711_712insC
|
XP_006717989.1:p.Ile238HisfsTer?
|
|
XM_011539981.1:c.756_757insC
|
XP_011538283.1:p.Ile253HisfsTer?
|
|
XM_011539982.1:c.660_661insC
|
XP_011538284.1:p.Ile221HisfsTer?
|
|
XR_945791.1:n.1326_1327insC
|
|
|
NM_000314.7:c.756_757insC
|
NP_000305.3:p.Ile253HisfsTer?
|
|
NM_001304717.5:c.1275_1276insC
|
NP_001291646.4:p.Ile426HisfsTer?
|
|
NM_001304718.2:c.165_166insC
|
NP_001291647.1:p.Ile56HisfsTer?
|
|
NM_000314.8:c.756_757insC
MANE Select
|
NP_000305.3:p.Ile253HisfsTer?
|
|