ENST00000559133.6:c.6998-152T>C
|
ENSP00000453958.2:n.6998-152T>C
|
|
ENST00000674301.2:c.*449-152T>C
|
ENSP00000501333.2:n.*449-152T>C
|
|
ENST00000682170.1:n.857T>C
|
|
|
ENST00000682767.1:n.233-152T>C
|
|
|
ENST00000316623.10:c.6997+251T>C
MANE Select
|
ENSP00000325527.5:n.6997+251T>C
|
|
ENST00000674301.1:c.2102-152T>C
|
ENSP00000501333.1:n.2102-152T>C
|
|
ENST00000316623.9:c.6997+251T>C
|
ENSP00000325527.5:n.6997+251T>C
|
|
ENST00000559133.5:c.2305-152T>C
|
|
|
ENST00000560720.1:n.535T>C
|
|
|
NM_000138.4:c.6997+251T>C , LRG_778t1:c.6997+251T>C
|
NP_000129.3:n.6997+251T>C
|
|
NM_000138.5:c.6997+251T>C
MANE Select
|
NP_000129.3:n.6997+251T>C
|
|