ENST00000559133.6:c.*688G=
|
ENSP00000453958.2:n.*688G=
|
|
ENST00000674301.2:c.*1393G=
|
ENSP00000501333.2:n.*1393G=
|
|
ENST00000682158.1:n.1261G=
|
|
|
ENST00000682170.1:n.2061G=
|
|
|
ENST00000682767.1:n.1177G=
|
|
|
ENST00000316623.10:c.7880G=
MANE Select
|
ENSP00000325527.5:p.Gly2627=
|
|
ENST00000674301.1:c.3046G=
|
ENSP00000501333.1:n.3046G=
|
|
ENST00000316623.9:c.7880G=
|
ENSP00000325527.5:p.Gly2627=
|
|
ENST00000559133.5:c.3249G=
|
|
|
ENST00000561429.1:n.135G=
|
|
|
NM_000138.4:c.7880G= , LRG_778t1:c.7880G=
|
NP_000129.3:p.Gly2627=
|
|
NM_000138.5:c.7880G=
MANE Select
|
NP_000129.3:p.Gly2627=
|
|