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NM_000138.5:c.7447T>A
MANE Select
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NP_000129.3:p.Cys2483Ser
|
|
ENST00000316623.10:c.7447T>A
MANE Select
|
ENSP00000325527.5:p.Cys2483Ser
|
|
NM_000138.4:c.7447T>A , LRG_778t1:c.7447T>A
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NP_000129.3:p.Cys2483Ser
|
|
ENST00000316623.9:c.7447T>A
|
ENSP00000325527.5:p.Cys2483Ser
|
|
ENST00000559133.5:c.2816T>A
|
|
|
ENST00000559133.6:c.*255T>A
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ENSP00000453958.2:n.*255T>A
|
|
ENST00000674301.1:c.2613T>A
|
ENSP00000501333.1:n.2613T>A
|
|
ENST00000674301.2:c.*960T>A
|
ENSP00000501333.2:n.*960T>A
|
|
ENST00000682170.1:n.1628T>A
|
|
|
ENST00000682767.1:n.744T>A
|
|