ENST00000426263.10:c.978T>A
MANE Select
|
ENSP00000416293.2:p.Phe326Leu
|
|
ENST00000674545.1:n.472T>A
|
|
|
ENST00000674765.1:c.978T>A
|
ENSP00000501811.1:p.Phe326Leu
|
|
ENST00000675112.1:n.1279T>A
|
|
|
ENST00000676254.1:n.1427T>A
|
|
|
ENST00000426263.7:c.978T>A
|
ENSP00000416293.2:p.Phe326Leu
|
|
ENST00000439722.2:c.857T>A
|
ENSP00000395521.2:n.857T>A
|
|
ENST00000475162.3:c.415+1598T>A
|
|
|
ENST00000630287.2:c.*293T>A
|
ENSP00000486694.1:n.*293T>A
|
|
NM_006516.2:c.978T>A
|
NP_006507.2:p.Phe326Leu
|
|
NM_006516.3:c.978T>A
|
NP_006507.2:p.Phe326Leu
|
|
NM_006516.4:c.978T>A
MANE Select
|
NP_006507.2:p.Phe326Leu
|
|