ENST00000298910.12:c.5021C>A
MANE Select
|
ENSP00000298910.7:p.Ser1674Tyr
|
|
ENST00000679360.1:c.*3930C>A
|
ENSP00000505368.1:n.*3930C>A
|
|
ENST00000679532.1:c.795C>A
|
|
|
ENST00000680018.1:c.466C>A
|
ENSP00000505347.1:n.466C>A
|
|
ENST00000680422.1:c.666C>A
|
|
|
ENST00000680425.1:c.188C>A
|
ENSP00000506459.1:n.188C>A
|
|
ENST00000680453.1:c.478C>A
|
|
|
ENST00000680790.1:c.4766C>A
|
ENSP00000505335.1:p.Ser1589Tyr
|
|
ENST00000681136.1:n.1005C>A
|
|
|
ENST00000681696.1:c.704C>A
|
ENSP00000505871.1:p.Ser235Tyr
|
|
ENST00000298910.11:c.5021C>A
|
ENSP00000298910.7:p.Ser1674Tyr
|
|
ENST00000430804.5:c.2317C>A
|
|
|
ENST00000479187.5:n.1702C>A
|
|
|
NM_198578.3:c.5021C>A
|
NP_940980.3:p.Ser1674Tyr
|
|
XM_005268629.2:c.5021C>A
|
XP_005268686.1:p.Ser1674Tyr
|
|
XM_011537877.1:c.5021C>A
|
XP_011536179.1:p.Ser1674Tyr
|
|
XM_011537878.1:c.5021C>A
|
XP_011536180.1:p.Ser1674Tyr
|
|
XM_011537879.1:c.3818C>A
|
XP_011536181.1:p.Ser1273Tyr
|
|
XM_011537881.1:c.4833C>A
|
XP_011536183.1:p.Val1611=
|
|
XM_005268629.4:c.5021C>A
|
XP_005268686.1:p.Ser1674Tyr
|
|
XM_011537877.3:c.5021C>A
|
XP_011536179.1:p.Ser1674Tyr
|
|
XM_011537881.3:c.4833C>A
|
XP_011536183.1:p.Val1611=
|
|
XM_017018787.1:c.1937C>A
|
XP_016874276.1:p.Ser646Tyr
|
|
XM_017018788.2:c.1283C>A
|
XP_016874277.1:p.Ser428Tyr
|
|
XM_024448833.1:c.3818C>A
|
XP_024304601.1:p.Ser1273Tyr
|
|
XR_001748574.2:n.5389C>A
|
|
|
NM_198578.4:c.5021C>A
MANE Select
|
NP_940980.4:p.Ser1674Tyr
|
|