ENST00000600737.6:c.3915A>G
MANE Select
|
ENSP00000473211.1:p.Gly1305=
|
|
ENST00000221249.10:c.3801A>G
|
ENSP00000221249.5:p.Gly1267=
|
|
ENST00000414982.7:c.3945A>G
|
ENSP00000407509.2:p.Gly1315=
|
|
ENST00000450331.7:c.3801A>G
|
ENSP00000394348.2:p.Gly1267=
|
|
ENST00000545201.6:c.3720A>G
|
ENSP00000443323.1:p.Gly1240=
|
|
ENST00000597202.1:n.273A>G
|
|
|
ENST00000599947.1:c.284A>G
|
|
|
ENST00000600737.5:c.3915A>G
|
ENSP00000473211.1:p.Gly1305=
|
|
NM_001166111.1:c.3945A>G
|
NP_001159583.1:p.Gly1315=
|
|
NM_001166112.1:c.3720A>G
|
NP_001159584.1:p.Gly1240=
|
|
NM_001166113.1:c.3801A>G
|
NP_001159585.1:p.Gly1267=
|
|
NM_001166114.1:c.3915A>G
|
NP_001159586.1:p.Gly1305=
|
|
NM_006702.4:c.3801A>G
|
NP_006693.3:p.Gly1267=
|
|
NM_001166111.2:c.3945A>G
|
NP_001159583.1:p.Gly1315=
|
|
NM_001166114.2:c.3915A>G
MANE Select
|
NP_001159586.1:p.Gly1305=
|
|
NM_006702.5:c.3801A>G
|
NP_006693.3:p.Gly1267=
|
|
NM_001166112.2:c.3720A>G
|
NP_001159584.1:p.Gly1240=
|
|