ENST00000298910.12:c.4941A>T
MANE Select
|
ENSP00000298910.7:p.Ser1647=
|
|
ENST00000679360.1:c.*3850A>T
|
ENSP00000505368.1:n.*3850A>T
|
|
ENST00000679532.1:c.715A>T
|
|
|
ENST00000680018.1:c.386A>T
|
ENSP00000505347.1:n.386A>T
|
|
ENST00000680422.1:c.586A>T
|
|
|
ENST00000680425.1:c.183-933A>T
|
ENSP00000506459.1:n.183-933A>T
|
|
ENST00000680453.1:c.473-933A>T
|
|
|
ENST00000680790.1:c.4686A>T
|
ENSP00000505335.1:p.Ser1562=
|
|
ENST00000681136.1:n.925A>T
|
|
|
ENST00000681696.1:c.624A>T
|
ENSP00000505871.1:p.Ser208=
|
|
ENST00000298910.11:c.4941A>T
|
ENSP00000298910.7:p.Ser1647=
|
|
ENST00000430804.5:c.2237A>T
|
|
|
ENST00000479187.5:n.1622A>T
|
|
|
NM_198578.3:c.4941A>T
|
NP_940980.3:p.Ser1647=
|
|
XM_005268629.2:c.4941A>T
|
XP_005268686.1:p.Ser1647=
|
|
XM_011537877.1:c.4941A>T
|
XP_011536179.1:p.Ser1647=
|
|
XM_011537878.1:c.4941A>T
|
XP_011536180.1:p.Ser1647=
|
|
XM_011537879.1:c.3738A>T
|
XP_011536181.1:p.Ser1246=
|
|
XM_011537881.1:c.4828-933A>T
|
XP_011536183.1:n.4828-933A>T
|
|
XM_005268629.4:c.4941A>T
|
XP_005268686.1:p.Ser1647=
|
|
XM_011537877.3:c.4941A>T
|
XP_011536179.1:p.Ser1647=
|
|
XM_011537881.3:c.4828-933A>T
|
XP_011536183.1:n.4828-933A>T
|
|
XM_017018787.1:c.1857A>T
|
XP_016874276.1:p.Ser619=
|
|
XM_017018788.2:c.1203A>T
|
XP_016874277.1:p.Ser401=
|
|
XM_024448833.1:c.3738A>T
|
XP_024304601.1:p.Ser1246=
|
|
XR_001748574.2:n.5309A>T
|
|
|
NM_198578.4:c.4941A>T
MANE Select
|
NP_940980.4:p.Ser1647=
|
|