ENST00000298910.12:c.4986A>G
MANE Select
|
ENSP00000298910.7:p.Ile1662Met
|
|
ENST00000679360.1:c.*3895A>G
|
ENSP00000505368.1:n.*3895A>G
|
|
ENST00000679532.1:c.760A>G
|
|
|
ENST00000680018.1:c.431A>G
|
ENSP00000505347.1:n.431A>G
|
|
ENST00000680422.1:c.631A>G
|
|
|
ENST00000680425.1:c.183-888A>G
|
ENSP00000506459.1:n.183-888A>G
|
|
ENST00000680453.1:c.473-888A>G
|
|
|
ENST00000680790.1:c.4731A>G
|
ENSP00000505335.1:p.Ile1577Met
|
|
ENST00000681136.1:n.970A>G
|
|
|
ENST00000681696.1:c.669A>G
|
ENSP00000505871.1:p.Ile223Met
|
|
ENST00000298910.11:c.4986A>G
|
ENSP00000298910.7:p.Ile1662Met
|
|
ENST00000430804.5:c.2282A>G
|
|
|
ENST00000479187.5:n.1667A>G
|
|
|
NM_198578.3:c.4986A>G
|
NP_940980.3:p.Ile1662Met
|
|
XM_005268629.2:c.4986A>G
|
XP_005268686.1:p.Ile1662Met
|
|
XM_011537877.1:c.4986A>G
|
XP_011536179.1:p.Ile1662Met
|
|
XM_011537878.1:c.4986A>G
|
XP_011536180.1:p.Ile1662Met
|
|
XM_011537879.1:c.3783A>G
|
XP_011536181.1:p.Ile1261Met
|
|
XM_011537881.1:c.4828-888A>G
|
XP_011536183.1:n.4828-888A>G
|
|
XM_005268629.4:c.4986A>G
|
XP_005268686.1:p.Ile1662Met
|
|
XM_011537877.3:c.4986A>G
|
XP_011536179.1:p.Ile1662Met
|
|
XM_011537881.3:c.4828-888A>G
|
XP_011536183.1:n.4828-888A>G
|
|
XM_017018787.1:c.1902A>G
|
XP_016874276.1:p.Ile634Met
|
|
XM_017018788.2:c.1248A>G
|
XP_016874277.1:p.Ile416Met
|
|
XM_024448833.1:c.3783A>G
|
XP_024304601.1:p.Ile1261Met
|
|
XR_001748574.2:n.5354A>G
|
|
|
NM_198578.4:c.4986A>G
MANE Select
|
NP_940980.4:p.Ile1662Met
|
|