ENST00000426263.10:c.1466A>T
MANE Select
|
ENSP00000416293.2:p.Asp489Val
|
|
ENST00000674545.1:n.2083A>T
|
|
|
ENST00000674765.1:c.1030-197A>T
|
ENSP00000501811.1:n.1030-197A>T
|
|
ENST00000675112.1:n.1767A>T
|
|
|
ENST00000676254.1:n.1915A>T
|
|
|
ENST00000426263.7:c.1466A>T
|
ENSP00000416293.2:p.Asp489Val
|
|
ENST00000475162.3:c.416-76A>T
|
|
|
ENST00000630287.2:c.*781A>T
|
ENSP00000486694.1:n.*781A>T
|
|
NM_006516.2:c.1466A>T
|
NP_006507.2:p.Asp489Val
|
|
NM_006516.3:c.1466A>T
|
NP_006507.2:p.Asp489Val
|
|
NM_006516.4:c.1466A>T
MANE Select
|
NP_006507.2:p.Asp489Val
|
|