ENST00000559133.6:c.*795T=
|
ENSP00000453958.2:n.*795T=
|
|
ENST00000674301.2:c.*1500T=
|
ENSP00000501333.2:n.*1500T=
|
|
ENST00000682158.1:n.1368T=
|
|
|
ENST00000682170.1:n.2168T=
|
|
|
ENST00000682767.1:n.1284T=
|
|
|
ENST00000316623.10:c.7987T=
MANE Select
|
ENSP00000325527.5:p.Cys2663=
|
|
ENST00000674301.1:c.3153T=
|
ENSP00000501333.1:n.3153T=
|
|
ENST00000316623.9:c.7987T=
|
ENSP00000325527.5:p.Cys2663=
|
|
ENST00000559133.5:c.3356T=
|
|
|
ENST00000561429.1:n.242T=
|
|
|
NM_000138.4:c.7987T= , LRG_778t1:c.7987T=
|
NP_000129.3:p.Cys2663=
|
|
NM_000138.5:c.7987T=
MANE Select
|
NP_000129.3:p.Cys2663=
|
|