|
NM_021939.4:c.591G>A
MANE Select
|
NP_068758.3:p.Lys197=
|
|
ENST00000321562.9:c.591G>A
MANE Select
|
ENSP00000317232.4:p.Lys197=
|
|
NM_021939.3:c.591G>A , LRG_12t1:c.591G>A
|
NP_068758.3:p.Lys197=
|
|
ENST00000321562.8:c.591G>A
|
ENSP00000317232.4:p.Lys197=
|
|
ENST00000489591.5:c.*1G>A
|
ENSP00000466352.1:n.*1G>A
|
|
ENST00000585664.5:c.411G>A
|
ENSP00000468703.1:p.Lys137=
|
|
ENST00000706683.1:c.591G>A
|
ENSP00000516497.1:p.Lys197=
|
|
XM_011525099.1:c.591G>A
|
XP_011523401.1:p.Lys197=
|
|
XM_011525099.3:c.591G>A
|
XP_011523401.1:p.Lys197=
|
|
XM_011525100.1:c.318G>A
|
XP_011523402.1:p.Lys106=
|
|
XM_011525100.2:c.318G>A
|
XP_011523402.1:p.Lys106=
|