ENST00000426263.10:c.922T>A
MANE Select
|
ENSP00000416293.2:p.Tyr308Asn
|
|
ENST00000674545.1:n.240T>A
|
|
|
ENST00000674765.1:c.922T>A
|
ENSP00000501811.1:p.Tyr308Asn
|
|
ENST00000675112.1:n.1223T>A
|
|
|
ENST00000676254.1:n.1371T>A
|
|
|
ENST00000426263.7:c.922T>A
|
ENSP00000416293.2:p.Tyr308Asn
|
|
ENST00000439722.2:c.801T>A
|
ENSP00000395521.2:n.801T>A
|
|
ENST00000475162.3:c.415+1366T>A
|
|
|
ENST00000630287.2:c.*237T>A
|
ENSP00000486694.1:n.*237T>A
|
|
NM_006516.2:c.922T>A
|
NP_006507.2:p.Tyr308Asn
|
|
NM_006516.3:c.922T>A
|
NP_006507.2:p.Tyr308Asn
|
|
NM_006516.4:c.922T>A
MANE Select
|
NP_006507.2:p.Tyr308Asn
|
|