ENST00000426263.10:c.939C>T
MANE Select
|
ENSP00000416293.2:p.Ser313=
|
|
ENST00000674545.1:n.257C>T
|
|
|
ENST00000674765.1:c.939C>T
|
ENSP00000501811.1:p.Ser313=
|
|
ENST00000675112.1:n.1240C>T
|
|
|
ENST00000676254.1:n.1388C>T
|
|
|
ENST00000426263.7:c.939C>T
|
ENSP00000416293.2:p.Ser313=
|
|
ENST00000439722.2:c.818C>T
|
ENSP00000395521.2:n.818C>T
|
|
ENST00000475162.3:c.415+1383C>T
|
|
|
ENST00000630287.2:c.*254C>T
|
ENSP00000486694.1:n.*254C>T
|
|
NM_006516.2:c.939C>T
|
NP_006507.2:p.Ser313=
|
|
NM_006516.3:c.939C>T
|
NP_006507.2:p.Ser313=
|
|
NM_006516.4:c.939C>T
MANE Select
|
NP_006507.2:p.Ser313=
|
|