|
ENST00000700029.2:c.964G>T
|
ENSP00000514759.2:p.Glu322Ter
|
|
|
ENST00000710265.1:c.871G>T
|
ENSP00000518161.1:p.Glu291Ter
|
|
|
ENST00000472832.3:c.871G>T
|
ENSP00000483066.2:p.Glu291Ter
|
|
|
ENST00000688158.2:n.1606G>T
|
|
|
|
ENST00000688922.2:c.*701G>T
|
ENSP00000508742.2:n.*701G>T
|
|
|
ENST00000700021.1:c.826G>T
|
ENSP00000514757.1:p.Glu276Ter
|
|
|
ENST00000700022.1:c.*210G>T
|
ENSP00000514758.1:n.*210G>T
|
|
|
ENST00000700023.1:n.2029G>T
|
|
|
|
ENST00000700024.1:n.2263G>T
|
|
|
|
ENST00000700025.1:n.1640G>T
|
|
|
|
ENST00000700026.1:n.508G>T
|
|
|
|
ENST00000700029.1:c.798G>T
|
|
|
|
ENST00000706954.1:c.871G>T
|
ENSP00000516674.1:p.Glu291Ter
|
|
|
ENST00000706955.1:c.*906G>T
|
ENSP00000516675.1:n.*906G>T
|
|
|
ENST00000686459.1:c.*457G>T
|
ENSP00000508909.1:n.*457G>T
|
|
|
ENST00000688158.1:c.*982G>T
|
ENSP00000509254.1:n.*982G>T
|
|
|
ENST00000688308.1:c.871G>T
|
ENSP00000508752.1:p.Glu291Ter
|
|
|
ENST00000688922.1:c.792G>T
|
|
|
|
ENST00000693560.1:c.1390G>T
|
ENSP00000509861.1:p.Glu464Ter
|
|
|
ENST00000371953.8:c.871G>T
MANE Select
|
ENSP00000361021.3:p.Glu291Ter
|
|
|
ENST00000371953.7:c.871G>T
|
ENSP00000361021.3:p.Glu291Ter
|
|
|
ENST00000472832.2:c.298G>T
|
ENSP00000483066.1:p.Glu100Ter
|
|
|
NM_000314.5:c.871G>T
|
NP_000305.3:p.Glu291Ter
|
|
|
NM_000314.6:c.871G>T
|
NP_000305.3:p.Glu291Ter
|
|
|
NM_001304717.2:c.1390G>T
|
NP_001291646.2:p.Glu464Ter
|
|
|
NM_001304718.1:c.280G>T
|
NP_001291647.1:p.Glu94Ter
|
|
|
XM_006717926.2:c.826G>T
|
XP_006717989.1:p.Glu276Ter
|
|
|
XM_011539981.1:c.871G>T
|
XP_011538283.1:p.Glu291Ter
|
|
|
XM_011539982.1:c.775G>T
|
XP_011538284.1:p.Glu259Ter
|
|
|
XR_945791.1:n.1441G>T
|
|
|
|
NM_000314.7:c.871G>T
|
NP_000305.3:p.Glu291Ter
|
|
|
NM_001304717.5:c.1390G>T
|
NP_001291646.4:p.Glu464Ter
|
|
|
NM_001304718.2:c.280G>T
|
NP_001291647.1:p.Glu94Ter
|
|
|
NM_000314.8:c.871G>T
MANE Select
|
NP_000305.3:p.Glu291Ter
|
|
