ENST00000559133.6:c.*1202A>G
|
ENSP00000453958.2:n.*1202A>G
|
|
ENST00000674301.2:c.*1907A>G
|
ENSP00000501333.2:n.*1907A>G
|
|
ENST00000682158.1:n.1775A>G
|
|
|
ENST00000682170.1:n.2575A>G
|
|
|
ENST00000682767.1:n.1691A>G
|
|
|
ENST00000316623.10:c.8394A>G
MANE Select
|
ENSP00000325527.5:p.Gly2798=
|
|
ENST00000674301.1:c.3560A>G
|
ENSP00000501333.1:n.3560A>G
|
|
ENST00000316623.9:c.8394A>G
|
ENSP00000325527.5:p.Gly2798=
|
|
ENST00000559133.5:c.3763A>G
|
|
|
ENST00000561429.1:n.649A>G
|
|
|
NM_000138.4:c.8394A>G , LRG_778t1:c.8394A>G
|
NP_000129.3:p.Gly2798=
|
|
NM_000138.5:c.8394A>G
MANE Select
|
NP_000129.3:p.Gly2798=
|
|