ENST00000426263.10:c.969G=
MANE Select
|
ENSP00000416293.2:p.Val323=
|
|
ENST00000674545.1:n.287G=
|
|
|
ENST00000674765.1:c.969G=
|
ENSP00000501811.1:p.Val323=
|
|
ENST00000675112.1:n.1270G=
|
|
|
ENST00000676254.1:n.1418G=
|
|
|
ENST00000426263.7:c.969G=
|
ENSP00000416293.2:p.Val323=
|
|
ENST00000439722.2:c.848G=
|
ENSP00000395521.2:n.848G=
|
|
ENST00000475162.3:c.415+1413G=
|
|
|
ENST00000630287.2:c.*284G=
|
ENSP00000486694.1:n.*284G=
|
|
NM_006516.2:c.969G=
|
NP_006507.2:p.Val323=
|
|
NM_006516.3:c.969G=
|
NP_006507.2:p.Val323=
|
|
NM_006516.4:c.969G=
MANE Select
|
NP_006507.2:p.Val323=
|
|