ENST00000426263.10:c.892T>A
MANE Select
|
ENSP00000416293.2:p.Phe298Ile
|
|
ENST00000674545.1:n.210T>A
|
|
|
ENST00000674765.1:c.892T>A
|
ENSP00000501811.1:p.Phe298Ile
|
|
ENST00000675112.1:n.1193T>A
|
|
|
ENST00000676254.1:n.1341T>A
|
|
|
ENST00000426263.7:c.892T>A
|
ENSP00000416293.2:p.Phe298Ile
|
|
ENST00000439722.2:c.771T>A
|
ENSP00000395521.2:n.771T>A
|
|
ENST00000475162.3:c.415+1336T>A
|
|
|
ENST00000630287.2:c.*207T>A
|
ENSP00000486694.1:n.*207T>A
|
|
NM_006516.2:c.892T>A
|
NP_006507.2:p.Phe298Ile
|
|
NM_006516.3:c.892T>A
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NP_006507.2:p.Phe298Ile
|
|
NM_006516.4:c.892T>A
MANE Select
|
NP_006507.2:p.Phe298Ile
|
|