|
ENST00000700029.2:c.922A>T
|
ENSP00000514759.2:p.Thr308Ser
|
|
|
ENST00000710265.1:c.829A>T
|
ENSP00000518161.1:p.Thr277Ser
|
|
|
ENST00000472832.3:c.829A>T
|
ENSP00000483066.2:p.Thr277Ser
|
|
|
ENST00000688158.2:n.1564A>T
|
|
|
|
ENST00000688922.2:c.*659A>T
|
ENSP00000508742.2:n.*659A>T
|
|
|
ENST00000700021.1:c.784A>T
|
ENSP00000514757.1:p.Thr262Ser
|
|
|
ENST00000700022.1:c.*168A>T
|
ENSP00000514758.1:n.*168A>T
|
|
|
ENST00000700023.1:n.1987A>T
|
|
|
|
ENST00000700024.1:n.2221A>T
|
|
|
|
ENST00000700025.1:n.1598A>T
|
|
|
|
ENST00000700026.1:n.466A>T
|
|
|
|
ENST00000700029.1:c.756A>T
|
|
|
|
ENST00000706954.1:c.829A>T
|
ENSP00000516674.1:p.Thr277Ser
|
|
|
ENST00000706955.1:c.*864A>T
|
ENSP00000516675.1:n.*864A>T
|
|
|
ENST00000686459.1:c.*415A>T
|
ENSP00000508909.1:n.*415A>T
|
|
|
ENST00000688158.1:c.*940A>T
|
ENSP00000509254.1:n.*940A>T
|
|
|
ENST00000688308.1:c.829A>T
|
ENSP00000508752.1:p.Thr277Ser
|
|
|
ENST00000688922.1:c.750A>T
|
|
|
|
ENST00000693560.1:c.1348A>T
|
ENSP00000509861.1:p.Thr450Ser
|
|
|
ENST00000371953.8:c.829A>T
MANE Select
|
ENSP00000361021.3:p.Thr277Ser
|
|
|
ENST00000371953.7:c.829A>T
|
ENSP00000361021.3:p.Thr277Ser
|
|
|
ENST00000472832.2:c.256A>T
|
ENSP00000483066.1:p.Thr86Ser
|
|
|
NM_000314.5:c.829A>T
|
NP_000305.3:p.Thr277Ser
|
|
|
NM_000314.6:c.829A>T
|
NP_000305.3:p.Thr277Ser
|
|
|
NM_001304717.2:c.1348A>T
|
NP_001291646.2:p.Thr450Ser
|
|
|
NM_001304718.1:c.238A>T
|
NP_001291647.1:p.Thr80Ser
|
|
|
XM_006717926.2:c.784A>T
|
XP_006717989.1:p.Thr262Ser
|
|
|
XM_011539981.1:c.829A>T
|
XP_011538283.1:p.Thr277Ser
|
|
|
XM_011539982.1:c.733A>T
|
XP_011538284.1:p.Thr245Ser
|
|
|
XR_945791.1:n.1399A>T
|
|
|
|
NM_000314.7:c.829A>T
|
NP_000305.3:p.Thr277Ser
|
|
|
NM_001304717.5:c.1348A>T
|
NP_001291646.4:p.Thr450Ser
|
|
|
NM_001304718.2:c.238A>T
|
NP_001291647.1:p.Thr80Ser
|
|
|
NM_000314.8:c.829A>T
MANE Select
|
NP_000305.3:p.Thr277Ser
|
|
