ENST00000559133.6:c.*1035-29A>G
|
ENSP00000453958.2:n.*1035-29A>G
|
|
ENST00000674301.2:c.*1740-29A>G
|
ENSP00000501333.2:n.*1740-29A>G
|
|
ENST00000682158.1:n.1608-29A>G
|
|
|
ENST00000682170.1:n.2408-29A>G
|
|
|
ENST00000682767.1:n.1524-29A>G
|
|
|
ENST00000316623.10:c.8227-29A>G
MANE Select
|
ENSP00000325527.5:n.8227-29A>G
|
|
ENST00000674301.1:c.3393-29A>G
|
ENSP00000501333.1:n.3393-29A>G
|
|
ENST00000316623.9:c.8227-29A>G
|
ENSP00000325527.5:n.8227-29A>G
|
|
ENST00000559133.5:c.3596-29A>G
|
|
|
ENST00000561429.1:n.482-29A>G
|
|
|
NM_000138.4:c.8227-29A>G , LRG_778t1:c.8227-29A>G
|
NP_000129.3:n.8227-29A>G
|
|
NM_000138.5:c.8227-29A>G
MANE Select
|
NP_000129.3:n.8227-29A>G
|
|