ENST00000426263.10:c.895G=
MANE Select
|
ENSP00000416293.2:p.Glu299=
|
|
ENST00000674545.1:n.213G=
|
|
|
ENST00000674765.1:c.895G=
|
ENSP00000501811.1:p.Glu299=
|
|
ENST00000675112.1:n.1196G=
|
|
|
ENST00000676254.1:n.1344G=
|
|
|
ENST00000426263.7:c.895G=
|
ENSP00000416293.2:p.Glu299=
|
|
ENST00000439722.2:c.774G=
|
ENSP00000395521.2:n.774G=
|
|
ENST00000475162.3:c.415+1339G=
|
|
|
ENST00000630287.2:c.*210G=
|
ENSP00000486694.1:n.*210G=
|
|
NM_006516.2:c.895G=
|
NP_006507.2:p.Glu299=
|
|
NM_006516.3:c.895G=
|
NP_006507.2:p.Glu299=
|
|
NM_006516.4:c.895G=
MANE Select
|
NP_006507.2:p.Glu299=
|
|