ENST00000600737.6:c.3919G=
MANE Select
|
ENSP00000473211.1:p.Glu1307=
|
|
ENST00000221249.10:c.3805G=
|
ENSP00000221249.5:p.Glu1269=
|
|
ENST00000414982.7:c.3949G=
|
ENSP00000407509.2:p.Glu1317=
|
|
ENST00000450331.7:c.3805G=
|
ENSP00000394348.2:p.Glu1269=
|
|
ENST00000545201.6:c.3724G=
|
ENSP00000443323.1:p.Glu1242=
|
|
ENST00000597202.1:n.277G=
|
|
|
ENST00000599947.1:c.288G=
|
|
|
ENST00000600737.5:c.3919G=
|
ENSP00000473211.1:p.Glu1307=
|
|
NM_001166111.1:c.3949G=
|
NP_001159583.1:p.Glu1317=
|
|
NM_001166112.1:c.3724G=
|
NP_001159584.1:p.Glu1242=
|
|
NM_001166113.1:c.3805G=
|
NP_001159585.1:p.Glu1269=
|
|
NM_001166114.1:c.3919G=
|
NP_001159586.1:p.Glu1307=
|
|
NM_006702.4:c.3805G=
|
NP_006693.3:p.Glu1269=
|
|
NM_001166111.2:c.3949G=
|
NP_001159583.1:p.Glu1317=
|
|
NM_001166114.2:c.3919G=
MANE Select
|
NP_001159586.1:p.Glu1307=
|
|
NM_006702.5:c.3805G=
|
NP_006693.3:p.Glu1269=
|
|
NM_001166112.2:c.3724G=
|
NP_001159584.1:p.Glu1242=
|
|