ENST00000559133.6:c.6998-141A>T
|
ENSP00000453958.2:n.6998-141A>T
|
|
ENST00000674301.2:c.*449-141A>T
|
ENSP00000501333.2:n.*449-141A>T
|
|
ENST00000682170.1:n.868A>T
|
|
|
ENST00000682767.1:n.233-141A>T
|
|
|
ENST00000316623.10:c.6997+262A>T
MANE Select
|
ENSP00000325527.5:n.6997+262A>T
|
|
ENST00000674301.1:c.2102-141A>T
|
ENSP00000501333.1:n.2102-141A>T
|
|
ENST00000316623.9:c.6997+262A>T
|
ENSP00000325527.5:n.6997+262A>T
|
|
ENST00000559133.5:c.2305-141A>T
|
|
|
ENST00000560720.1:n.546A>T
|
|
|
NM_000138.4:c.6997+262A>T , LRG_778t1:c.6997+262A>T
|
NP_000129.3:n.6997+262A>T
|
|
NM_000138.5:c.6997+262A>T
MANE Select
|
NP_000129.3:n.6997+262A>T
|
|