ENST00000559133.6:c.*879G=
|
ENSP00000453958.2:n.*879G=
|
|
ENST00000674301.2:c.*1584G=
|
ENSP00000501333.2:n.*1584G=
|
|
ENST00000682158.1:n.1452G=
|
|
|
ENST00000682170.1:n.2252G=
|
|
|
ENST00000682767.1:n.1368G=
|
|
|
ENST00000316623.10:c.8071G=
MANE Select
|
ENSP00000325527.5:p.Gly2691=
|
|
ENST00000674301.1:c.3237G=
|
ENSP00000501333.1:n.3237G=
|
|
ENST00000316623.9:c.8071G=
|
ENSP00000325527.5:p.Gly2691=
|
|
ENST00000559133.5:c.3440G=
|
|
|
ENST00000561429.1:n.326G=
|
|
|
NM_000138.4:c.8071G= , LRG_778t1:c.8071G=
|
NP_000129.3:p.Gly2691=
|
|
NM_000138.5:c.8071G=
MANE Select
|
NP_000129.3:p.Gly2691=
|
|