|
ENST00000700029.2:c.988G>T
|
ENSP00000514759.2:p.Glu330Ter
|
|
|
ENST00000710265.1:c.895G>T
|
ENSP00000518161.1:p.Glu299Ter
|
|
|
ENST00000472832.3:c.895G>T
|
ENSP00000483066.2:p.Glu299Ter
|
|
|
ENST00000688158.2:n.1630G>T
|
|
|
|
ENST00000688922.2:c.*725G>T
|
ENSP00000508742.2:n.*725G>T
|
|
|
ENST00000700021.1:c.850G>T
|
ENSP00000514757.1:p.Glu284Ter
|
|
|
ENST00000700022.1:c.*234G>T
|
ENSP00000514758.1:n.*234G>T
|
|
|
ENST00000700023.1:n.2053G>T
|
|
|
|
ENST00000700024.1:n.2287G>T
|
|
|
|
ENST00000700025.1:n.1664G>T
|
|
|
|
ENST00000700026.1:n.532G>T
|
|
|
|
ENST00000706954.1:c.895G>T
|
ENSP00000516674.1:p.Glu299Ter
|
|
|
ENST00000706955.1:c.*930G>T
|
ENSP00000516675.1:n.*930G>T
|
|
|
ENST00000686459.1:c.*481G>T
|
ENSP00000508909.1:n.*481G>T
|
|
|
ENST00000688158.1:c.*1006G>T
|
ENSP00000509254.1:n.*1006G>T
|
|
|
ENST00000688308.1:c.895G>T
|
ENSP00000508752.1:p.Glu299Ter
|
|
|
ENST00000688922.1:c.816G>T
|
|
|
|
ENST00000693560.1:c.1414G>T
|
ENSP00000509861.1:p.Glu472Ter
|
|
|
ENST00000371953.8:c.895G>T
MANE Select
|
ENSP00000361021.3:p.Glu299Ter
|
|
|
ENST00000371953.7:c.895G>T
|
ENSP00000361021.3:p.Glu299Ter
|
|
|
ENST00000472832.2:c.322G>T
|
ENSP00000483066.1:p.Glu108Ter
|
|
|
NM_000314.5:c.895G>T
|
NP_000305.3:p.Glu299Ter
|
|
|
NM_000314.6:c.895G>T
|
NP_000305.3:p.Glu299Ter
|
|
|
NM_001304717.2:c.1414G>T
|
NP_001291646.2:p.Glu472Ter
|
|
|
NM_001304718.1:c.304G>T
|
NP_001291647.1:p.Glu102Ter
|
|
|
XM_006717926.2:c.850G>T
|
XP_006717989.1:p.Glu284Ter
|
|
|
XM_011539981.1:c.895G>T
|
XP_011538283.1:p.Glu299Ter
|
|
|
XM_011539982.1:c.799G>T
|
XP_011538284.1:p.Glu267Ter
|
|
|
XR_945791.1:n.1465G>T
|
|
|
|
NM_000314.7:c.895G>T
|
NP_000305.3:p.Glu299Ter
|
|
|
NM_001304717.5:c.1414G>T
|
NP_001291646.4:p.Glu472Ter
|
|
|
NM_001304718.2:c.304G>T
|
NP_001291647.1:p.Glu102Ter
|
|
|
NM_000314.8:c.895G>T
MANE Select
|
NP_000305.3:p.Glu299Ter
|
|
