ENST00000298910.12:c.7140T>G
MANE Select
|
ENSP00000298910.7:p.Thr2380=
|
|
ENST00000636518.1:c.937T>G
|
|
|
ENST00000679360.1:c.*6049T>G
|
ENSP00000505368.1:n.*6049T>G
|
|
ENST00000679532.1:c.2914T>G
|
|
|
ENST00000679683.1:c.930T>G
|
|
|
ENST00000680018.1:c.2585T>G
|
ENSP00000505347.1:n.2585T>G
|
|
ENST00000680422.1:c.4227T>G
|
|
|
ENST00000680425.1:c.2307T>G
|
ENSP00000506459.1:n.2307T>G
|
|
ENST00000680453.1:c.2597T>G
|
|
|
ENST00000680790.1:c.6885T>G
|
ENSP00000505335.1:p.Thr2295=
|
|
ENST00000681136.1:n.3124T>G
|
|
|
ENST00000681696.1:c.2823T>G
|
ENSP00000505871.1:p.Thr941=
|
|
ENST00000681773.1:n.347T>G
|
|
|
ENST00000298910.11:c.7140T>G
|
ENSP00000298910.7:p.Thr2380=
|
|
ENST00000430804.5:c.4436T>G
|
|
|
ENST00000479187.5:n.3821T>G
|
|
|
NM_198578.3:c.7140T>G
|
NP_940980.3:p.Thr2380=
|
|
XM_005268629.2:c.7140T>G
|
XP_005268686.1:p.Thr2380=
|
|
XM_011537877.1:c.7140T>G
|
XP_011536179.1:p.Thr2380=
|
|
XM_011537879.1:c.5937T>G
|
XP_011536181.1:p.Thr1979=
|
|
XR_944868.1:n.485-8686A>C
|
|
|
XM_005268629.4:c.7140T>G
|
XP_005268686.1:p.Thr2380=
|
|
XM_011537877.3:c.7140T>G
|
XP_011536179.1:p.Thr2380=
|
|
XM_017018787.1:c.4056T>G
|
XP_016874276.1:p.Thr1352=
|
|
XM_017018788.2:c.3402T>G
|
XP_016874277.1:p.Thr1134=
|
|
XM_024448833.1:c.5937T>G
|
XP_024304601.1:p.Thr1979=
|
|
XR_944868.2:n.485-8686A>C
|
|
|
NM_198578.4:c.7140T>G
MANE Select
|
NP_940980.4:p.Thr2380=
|
|