ENST00000430710.8:c.324A>C
|
ENSP00000406288.3:p.Gly108=
|
|
ENST00000553651.2:n.2967A>C
|
|
|
ENST00000555962.6:c.-111+2793A>C
|
ENSP00000495174.1:n.-111+2793A>C
|
|
ENST00000557364.6:c.1161A>C
|
ENSP00000451601.1:p.Gly387=
|
|
ENST00000642518.1:c.324A>C
|
ENSP00000496722.1:p.Gly108=
|
|
ENST00000643048.1:n.1456A>C
|
|
|
ENST00000643469.1:c.1161A>C
|
ENSP00000495070.1:p.Gly387=
|
|
ENST00000645140.1:c.1073A>C
|
|
|
ENST00000645929.1:c.324A>C
|
ENSP00000494402.1:p.Gly108=
|
|
ENST00000646063.1:c.1248A>C
|
ENSP00000496565.1:p.Gly416=
|
|
ENST00000646340.1:c.1167A>C
|
ENSP00000496730.1:p.Gly389=
|
|
ENST00000646647.2:c.1161A>C
MANE Select
|
ENSP00000495240.1:p.Gly387=
|
|
ENST00000399982.6:c.1161A>C
|
ENSP00000382863.2:p.Gly387=
|
|
ENST00000430710.7:c.324A>C
|
ENSP00000406288.3:p.Gly108=
|
|
ENST00000555962.5:n.150+2793A>C
|
|
|
ENST00000557364.5:c.1161A>C
|
ENSP00000451601.1:p.Gly387=
|
|
NM_001170629.1:c.1161A>C
|
NP_001164100.1:p.Gly387=
|
|
NM_020920.3:c.324A>C
|
NP_065971.2:p.Gly108=
|
|
NM_001170629.2:c.1161A>C
MANE Select
|
NP_001164100.1:p.Gly387=
|
|
NM_020920.4:c.324A>C
|
NP_065971.2:p.Gly108=
|
|