ENST00000559133.6:c.*792G>T
|
ENSP00000453958.2:n.*792G>T
|
|
ENST00000674301.2:c.*1497G>T
|
ENSP00000501333.2:n.*1497G>T
|
|
ENST00000682158.1:n.1365G>T
|
|
|
ENST00000682170.1:n.2165G>T
|
|
|
ENST00000682767.1:n.1281G>T
|
|
|
ENST00000316623.10:c.7984G>T
MANE Select
|
ENSP00000325527.5:p.Gly2662Cys
|
|
ENST00000674301.1:c.3150G>T
|
ENSP00000501333.1:n.3150G>T
|
|
ENST00000316623.9:c.7984G>T
|
ENSP00000325527.5:p.Gly2662Cys
|
|
ENST00000559133.5:c.3353G>T
|
|
|
ENST00000561429.1:n.239G>T
|
|
|
NM_000138.4:c.7984G>T , LRG_778t1:c.7984G>T
|
NP_000129.3:p.Gly2662Cys
|
|
NM_000138.5:c.7984G>T
MANE Select
|
NP_000129.3:p.Gly2662Cys
|
|