ENST00000559133.6:c.*1279C>A
|
ENSP00000453958.2:n.*1279C>A
|
|
ENST00000674301.2:c.*1984C>A
|
ENSP00000501333.2:n.*1984C>A
|
|
ENST00000682158.1:n.1852C>A
|
|
|
ENST00000682170.1:n.2652C>A
|
|
|
ENST00000682767.1:n.1768C>A
|
|
|
ENST00000316623.10:c.8471C>A
MANE Select
|
ENSP00000325527.5:p.Ala2824Asp
|
|
ENST00000674301.1:c.3637C>A
|
ENSP00000501333.1:n.3637C>A
|
|
ENST00000316623.9:c.8471C>A
|
ENSP00000325527.5:p.Ala2824Asp
|
|
ENST00000559133.5:c.3840C>A
|
|
|
NM_000138.4:c.8471C>A , LRG_778t1:c.8471C>A
|
NP_000129.3:p.Ala2824Asp
|
|
NM_000138.5:c.8471C>A
MANE Select
|
NP_000129.3:p.Ala2824Asp
|
|