ENST00000342695.9:c.969T>G
MANE Select
|
ENSP00000339182.4:p.Thr323=
|
|
ENST00000295548.3:c.969T>G
|
ENSP00000295548.3:p.Thr323=
|
|
ENST00000342695.8:c.969T>G
|
ENSP00000339182.4:p.Thr323=
|
|
ENST00000392443.7:c.969T>G
|
ENSP00000376238.3:p.Thr323=
|
|
ENST00000450950.6:c.*412T>G
|
ENSP00000402023.2:n.*412T>G
|
|
ENST00000490925.5:n.1077T>G
|
|
|
NM_032279.3:c.969T>G
|
NP_115655.2:p.Thr323=
|
|
XM_005247829.2:c.969T>G
|
XP_005247886.1:p.Thr323=
|
|
XM_011513232.1:c.969T>G
|
XP_011511534.1:p.Thr323=
|
|
XR_241512.2:n.1270T>G
|
|
|
XR_924191.1:n.1270T>G
|
|
|
XM_011513232.2:c.969T>G
|
XP_011511534.1:p.Thr323=
|
|
XM_017007318.1:c.642T>G
|
XP_016862807.1:p.Thr214=
|
|
XM_017007319.1:c.969T>G
|
XP_016862808.1:p.Thr323=
|
|
XR_001740324.2:n.1039T>G
|
|
|
XR_001740325.1:n.1039T>G
|
|
|
XR_002959602.1:n.1203T>G
|
|
|
XR_924191.3:n.1039T>G
|
|
|
NM_032279.4:c.969T>G
MANE Select
|
NP_115655.2:p.Thr323=
|
|