ENST00000559133.6:c.*821G>A
|
ENSP00000453958.2:n.*821G>A
|
|
ENST00000674301.2:c.*1526G>A
|
ENSP00000501333.2:n.*1526G>A
|
|
ENST00000682158.1:n.1394G>A
|
|
|
ENST00000682170.1:n.2194G>A
|
|
|
ENST00000682767.1:n.1310G>A
|
|
|
ENST00000316623.10:c.8013G>A
MANE Select
|
ENSP00000325527.5:p.Leu2671=
|
|
ENST00000674301.1:c.3179G>A
|
ENSP00000501333.1:n.3179G>A
|
|
ENST00000316623.9:c.8013G>A
|
ENSP00000325527.5:p.Leu2671=
|
|
ENST00000559133.5:c.3382G>A
|
|
|
ENST00000561429.1:n.268G>A
|
|
|
NM_000138.4:c.8013G>A , LRG_778t1:c.8013G>A
|
NP_000129.3:p.Leu2671=
|
|
NM_000138.5:c.8013G>A
MANE Select
|
NP_000129.3:p.Leu2671=
|
|