ENST00000426263.10:c.1276G>A
MANE Select
|
ENSP00000416293.2:p.Glu426Lys
|
|
ENST00000674545.1:n.1893G>A
|
|
|
ENST00000674765.1:c.1030-750G>A
|
ENSP00000501811.1:n.1030-750G>A
|
|
ENST00000675112.1:n.1577G>A
|
|
|
ENST00000676254.1:n.1725G>A
|
|
|
ENST00000426263.7:c.1276G>A
|
ENSP00000416293.2:p.Glu426Lys
|
|
ENST00000475162.3:c.416-629G>A
|
|
|
ENST00000630287.2:c.*591G>A
|
ENSP00000486694.1:n.*591G>A
|
|
NM_006516.2:c.1276G>A
|
NP_006507.2:p.Glu426Lys
|
|
NM_006516.3:c.1276G>A
|
NP_006507.2:p.Glu426Lys
|
|
NM_006516.4:c.1276G>A
MANE Select
|
NP_006507.2:p.Glu426Lys
|
|