ENST00000356839.10:c.630T>C
MANE Select
|
ENSP00000349297.5:p.Thr210=
|
|
ENST00000322910.9:c.*585T>C
|
ENSP00000325395.5:n.*585T>C
|
|
ENST00000350303.9:c.564T>C
|
ENSP00000344152.5:p.Thr188=
|
|
ENST00000356839.9:c.630T>C
|
ENSP00000349297.5:p.Thr210=
|
|
ENST00000543245.6:c.699T>C
|
ENSP00000438689.2:p.Thr233=
|
|
ENST00000577191.5:n.707T>C
|
|
|
ENST00000577857.5:n.446T>C
|
|
|
ENST00000579286.5:n.811T>C
|
|
|
ENST00000580365.1:n.361T>C
|
|
|
ENST00000581378.5:c.348T>C
|
|
|
ENST00000581562.5:n.532T>C
|
|
|
ENST00000582379.1:n.14T>C
|
|
|
ENST00000583312.5:c.645T>C
|
ENSP00000467920.1:p.Thr215=
|
|
ENST00000583760.1:n.412T>C
|
|
|
NM_000018.3:c.630T>C
|
NP_000009.1:p.Thr210=
|
|
NM_001033859.2:c.564T>C
|
NP_001029031.1:p.Thr188=
|
|
NM_001270447.1:c.699T>C
|
NP_001257376.1:p.Thr233=
|
|
NM_001270448.1:c.402T>C
|
NP_001257377.1:p.Thr134=
|
|
XM_006721516.2:c.630T>C
|
XP_006721579.2:p.Thr210=
|
|
XM_011523829.1:c.630T>C
|
XP_011522131.1:p.Thr210=
|
|
XM_011523830.1:c.630T>C
|
XP_011522132.1:p.Thr210=
|
|
XR_934021.1:n.737T>C
|
|
|
XR_934022.1:n.737T>C
|
|
|
XR_934023.1:n.737T>C
|
|
|
XM_006721516.3:c.630T>C
|
XP_006721579.2:p.Thr210=
|
|
XM_011523829.2:c.630T>C
|
XP_011522131.1:p.Thr210=
|
|
XM_011523830.2:c.630T>C
|
XP_011522132.1:p.Thr210=
|
|
XM_024450741.1:c.630T>C
|
XP_024306509.1:p.Thr210=
|
|
XR_934021.2:n.689T>C
|
|
|
XR_934022.2:n.689T>C
|
|
|
XR_934023.2:n.689T>C
|
|
|
NM_000018.4:c.630T>C
MANE Select
|
NP_000009.1:p.Thr210=
|
|
NM_001033859.3:c.564T>C
|
NP_001029031.1:p.Thr188=
|
|
NM_001270447.2:c.699T>C
|
NP_001257376.1:p.Thr233=
|
|
NM_001270448.2:c.402T>C
|
NP_001257377.1:p.Thr134=
|
|