ENST00000426263.10:c.979G>A
MANE Select
|
ENSP00000416293.2:p.Val327Met
|
|
ENST00000674545.1:n.473G>A
|
|
|
ENST00000674765.1:c.979G>A
|
ENSP00000501811.1:p.Val327Met
|
|
ENST00000675112.1:n.1280G>A
|
|
|
ENST00000676254.1:n.1428G>A
|
|
|
ENST00000426263.7:c.979G>A
|
ENSP00000416293.2:p.Val327Met
|
|
ENST00000439722.2:c.858G>A
|
ENSP00000395521.2:n.858G>A
|
|
ENST00000475162.3:c.415+1599G>A
|
|
|
ENST00000630287.2:c.*294G>A
|
ENSP00000486694.1:n.*294G>A
|
|
NM_006516.2:c.979G>A
|
NP_006507.2:p.Val327Met
|
|
NM_006516.3:c.979G>A
|
NP_006507.2:p.Val327Met
|
|
NM_006516.4:c.979G>A
MANE Select
|
NP_006507.2:p.Val327Met
|
|