ENST00000298910.12:c.6032T>G
MANE Select
|
ENSP00000298910.7:p.Ile2011Ser
|
|
ENST00000679360.1:c.*4941T>G
|
ENSP00000505368.1:n.*4941T>G
|
|
ENST00000679532.1:c.1806T>G
|
|
|
ENST00000680018.1:c.1477T>G
|
ENSP00000505347.1:n.1477T>G
|
|
ENST00000680422.1:c.1677T>G
|
|
|
ENST00000680425.1:c.1199T>G
|
ENSP00000506459.1:n.1199T>G
|
|
ENST00000680453.1:c.1489T>G
|
|
|
ENST00000680790.1:c.5777T>G
|
ENSP00000505335.1:p.Ile1926Ser
|
|
ENST00000681136.1:n.2016T>G
|
|
|
ENST00000681696.1:c.1715T>G
|
ENSP00000505871.1:p.Ile572Ser
|
|
ENST00000298910.11:c.6032T>G
|
ENSP00000298910.7:p.Ile2011Ser
|
|
ENST00000430804.5:c.3328T>G
|
|
|
ENST00000479187.5:n.2713T>G
|
|
|
NM_198578.3:c.6032T>G
|
NP_940980.3:p.Ile2011Ser
|
|
XM_005268629.2:c.6032T>G
|
XP_005268686.1:p.Ile2011Ser
|
|
XM_011537877.1:c.6032T>G
|
XP_011536179.1:p.Ile2011Ser
|
|
XM_011537878.1:c.6032T>G
|
XP_011536180.1:p.Ile2011Ser
|
|
XM_011537879.1:c.4829T>G
|
XP_011536181.1:p.Ile1610Ser
|
|
XM_005268629.4:c.6032T>G
|
XP_005268686.1:p.Ile2011Ser
|
|
XM_011537877.3:c.6032T>G
|
XP_011536179.1:p.Ile2011Ser
|
|
XM_017018787.1:c.2948T>G
|
XP_016874276.1:p.Ile983Ser
|
|
XM_017018788.2:c.2294T>G
|
XP_016874277.1:p.Ile765Ser
|
|
XM_024448833.1:c.4829T>G
|
XP_024304601.1:p.Ile1610Ser
|
|
NM_198578.4:c.6032T>G
MANE Select
|
NP_940980.4:p.Ile2011Ser
|
|