ENST00000559133.6:c.*1100dup
|
ENSP00000453958.2:n.*1100dup
|
|
ENST00000674301.2:c.*1805dup
|
ENSP00000501333.2:n.*1805dup
|
|
ENST00000682158.1:n.1673dup
|
|
|
ENST00000682170.1:n.2473dup
|
|
|
ENST00000682767.1:n.1589dup
|
|
|
ENST00000316623.10:c.8292dup
MANE Select
|
ENSP00000325527.5:p.Ala2765CysfsTer9
|
|
ENST00000674301.1:c.3458dup
|
ENSP00000501333.1:n.3458dup
|
|
ENST00000316623.9:c.8292dup
|
ENSP00000325527.5:p.Ala2765CysfsTer9
|
|
ENST00000559133.5:c.3661dup
|
|
|
ENST00000561429.1:n.547dup
|
|
|
NM_000138.4:c.8292dup , LRG_778t1:c.8292dup
|
NP_000129.3:p.Ala2765CysfsTer9
|
|
NM_000138.5:c.8292dup
MANE Select
|
NP_000129.3:p.Ala2765CysfsTer9
|
|