ENST00000247933.9:c.826G>T
|
ENSP00000247933.4:p.Glu276Ter
|
|
ENST00000514224.2:c.826G>T
MANE Select
|
ENSP00000425081.2:p.Glu276Ter
|
|
ENST00000652070.1:n.882G>T
|
|
|
ENST00000247933.8:c.826G>T
|
ENSP00000247933.4:p.Glu276Ter
|
|
ENST00000514192.5:c.643G>T
|
ENSP00000423685.1:p.Glu215Ter
|
|
ENST00000514224.1:c.430G>T
|
ENSP00000425081.1:p.Glu144Ter
|
|
ENST00000514698.5:n.826G>T
|
|
|
NM_000203.4:c.826G>T
|
NP_000194.2:p.Glu276Ter
|
|
NR_110313.1:n.914G>T
|
|
|
XM_006713882.2:c.430G>T
|
XP_006713945.1:p.Glu144Ter
|
|
XM_011513459.1:c.785G>T
|
XP_011511761.1:p.Gly262Val
|
|
XM_011513460.1:c.685G>T
|
XP_011511762.1:p.Glu229Ter
|
|
XM_011513461.1:c.619G>T
|
XP_011511763.1:p.Glu207Ter
|
|
XM_011513462.1:c.538G>T
|
XP_011511764.1:p.Glu180Ter
|
|
XM_011513463.1:c.538G>T
|
XP_011511765.1:p.Glu180Ter
|
|
XR_924947.1:n.895G>T
|
|
|
NM_000203.5:c.826G>T
MANE Select
|
NP_000194.2:p.Glu276Ter
|
|
NM_001363576.1:c.430G>T
|
NP_001350505.1:p.Glu144Ter
|
|
XM_011513461.2:c.619G>T
|
XP_011511763.1:p.Glu207Ter
|
|
XM_017008163.1:c.-135G>T
|
XP_016863652.1:n.-135G>T
|
|