ENST00000559133.6:c.*1236G>T
|
ENSP00000453958.2:n.*1236G>T
|
|
ENST00000674301.2:c.*1941G>T
|
ENSP00000501333.2:n.*1941G>T
|
|
ENST00000682158.1:n.1809G>T
|
|
|
ENST00000682170.1:n.2609G>T
|
|
|
ENST00000682767.1:n.1725G>T
|
|
|
ENST00000316623.10:c.8428G>T
MANE Select
|
ENSP00000325527.5:p.Glu2810Ter
|
|
ENST00000674301.1:c.3594G>T
|
ENSP00000501333.1:n.3594G>T
|
|
ENST00000316623.9:c.8428G>T
|
ENSP00000325527.5:p.Glu2810Ter
|
|
ENST00000559133.5:c.3797G>T
|
|
|
NM_000138.4:c.8428G>T , LRG_778t1:c.8428G>T
|
NP_000129.3:p.Glu2810Ter
|
|
NM_000138.5:c.8428G>T
MANE Select
|
NP_000129.3:p.Glu2810Ter
|
|