ENST00000559133.6:c.*1148C>G
|
ENSP00000453958.2:n.*1148C>G
|
|
ENST00000674301.2:c.*1853C>G
|
ENSP00000501333.2:n.*1853C>G
|
|
ENST00000682158.1:n.1721C>G
|
|
|
ENST00000682170.1:n.2521C>G
|
|
|
ENST00000682767.1:n.1637C>G
|
|
|
ENST00000316623.10:c.8340C>G
MANE Select
|
ENSP00000325527.5:p.Leu2780=
|
|
ENST00000674301.1:c.3506C>G
|
ENSP00000501333.1:n.3506C>G
|
|
ENST00000316623.9:c.8340C>G
|
ENSP00000325527.5:p.Leu2780=
|
|
ENST00000559133.5:c.3709C>G
|
|
|
ENST00000561429.1:n.595C>G
|
|
|
NM_000138.4:c.8340C>G , LRG_778t1:c.8340C>G
|
NP_000129.3:p.Leu2780=
|
|
NM_000138.5:c.8340C>G
MANE Select
|
NP_000129.3:p.Leu2780=
|
|