ENST00000559133.6:c.6998-137A>G
|
ENSP00000453958.2:n.6998-137A>G
|
|
ENST00000674301.2:c.*449-137A>G
|
ENSP00000501333.2:n.*449-137A>G
|
|
ENST00000682170.1:n.872A>G
|
|
|
ENST00000682767.1:n.233-137A>G
|
|
|
ENST00000316623.10:c.6997+266A>G
MANE Select
|
ENSP00000325527.5:n.6997+266A>G
|
|
ENST00000674301.1:c.2102-137A>G
|
ENSP00000501333.1:n.2102-137A>G
|
|
ENST00000316623.9:c.6997+266A>G
|
ENSP00000325527.5:n.6997+266A>G
|
|
ENST00000559133.5:c.2305-137A>G
|
|
|
ENST00000560720.1:n.550A>G
|
|
|
NM_000138.4:c.6997+266A>G , LRG_778t1:c.6997+266A>G
|
NP_000129.3:n.6997+266A>G
|
|
NM_000138.5:c.6997+266A>G
MANE Select
|
NP_000129.3:n.6997+266A>G
|
|