ENST00000559133.6:c.*700G=
|
ENSP00000453958.2:n.*700G=
|
|
ENST00000674301.2:c.*1405G=
|
ENSP00000501333.2:n.*1405G=
|
|
ENST00000682158.1:n.1273G=
|
|
|
ENST00000682170.1:n.2073G=
|
|
|
ENST00000682767.1:n.1189G=
|
|
|
ENST00000316623.10:c.7892G=
MANE Select
|
ENSP00000325527.5:p.Cys2631=
|
|
ENST00000674301.1:c.3058G=
|
ENSP00000501333.1:n.3058G=
|
|
ENST00000316623.9:c.7892G=
|
ENSP00000325527.5:p.Cys2631=
|
|
ENST00000559133.5:c.3261G=
|
|
|
ENST00000561429.1:n.147G=
|
|
|
NM_000138.4:c.7892G= , LRG_778t1:c.7892G=
|
NP_000129.3:p.Cys2631=
|
|
NM_000138.5:c.7892G=
MANE Select
|
NP_000129.3:p.Cys2631=
|
|