ENST00000317961.9:c.3645T>C
MANE Select
|
ENSP00000322408.4:p.Thr1215=
|
|
ENST00000317961.8:c.3645T>C
|
ENSP00000322408.4:p.Thr1215=
|
|
ENST00000382806.6:c.3474T>C
|
ENSP00000372256.2:p.Thr1158=
|
|
ENST00000415360.1:c.561T>C
|
ENSP00000389433.1:p.Thr187=
|
|
ENST00000440077.5:c.3522T>C
|
ENSP00000398543.1:p.Thr1174=
|
|
ENST00000469599.6:n.2243T>C
|
|
|
ENST00000492117.1:n.3537T>C
|
|
|
ENST00000541639.5:c.3738T>C
|
ENSP00000444293.1:p.Thr1246=
|
|
NM_001146705.1:c.3738T>C
|
NP_001140177.1:p.Thr1246=
|
|
NM_001146706.1:c.3474T>C
|
NP_001140178.1:p.Thr1158=
|
|
NM_004653.4:c.3645T>C
|
NP_004644.2:p.Thr1215=
|
|
XM_005262560.1:c.3510T>C
|
XP_005262617.1:p.Thr1170=
|
|
XM_005262561.1:c.3414T>C
|
XP_005262618.1:p.Thr1138=
|
|
XM_011531468.1:c.3567T>C
|
XP_011529770.1:p.Thr1189=
|
|
XR_244571.2:n.3933T>C
|
|
|
XR_430568.2:n.4267T>C
|
|
|
XM_005262560.3:c.3510T>C
|
XP_005262617.1:p.Thr1170=
|
|
XM_005262561.3:c.3414T>C
|
XP_005262618.1:p.Thr1138=
|
|
XM_011531468.3:c.3567T>C
|
XP_011529770.1:p.Thr1189=
|
|
XM_024452495.1:c.1635T>C
|
XP_024308263.1:p.Thr545=
|
|
XM_024452496.1:c.1401T>C
|
XP_024308264.1:p.Thr467=
|
|
XR_001756009.2:n.4383T>C
|
|
|
XR_001756010.2:n.4383T>C
|
|
|
XR_001756011.2:n.4248T>C
|
|
|
XR_001756012.2:n.4396T>C
|
|
|
XR_001756013.2:n.3714T>C
|
|
|
XR_002958832.1:n.3815T>C
|
|
|
XR_002958834.1:n.4039T>C
|
|
|
XR_002958835.1:n.3922T>C
|
|
|
XR_002958836.1:n.4605T>C
|
|
|
XR_002958837.1:n.4412T>C
|
|
|
XR_244571.4:n.3932T>C
|
|
|
XR_430568.4:n.4266T>C
|
|
|
NM_001146706.2:c.3474T>C
|
NP_001140178.1:p.Thr1158=
|
|
NM_004653.5:c.3645T>C
MANE Select
|
NP_004644.2:p.Thr1215=
|
|
NM_001146705.2:c.3738T>C
|
NP_001140177.1:p.Thr1246=
|
|