ENST00000559133.6:c.6891G>A
|
ENSP00000453958.2:p.Thr2297=
|
|
ENST00000674301.2:c.*342G>A
|
ENSP00000501333.2:n.*342G>A
|
|
ENST00000682170.1:n.500G>A
|
|
|
ENST00000682767.1:n.126G>A
|
|
|
ENST00000316623.10:c.6891G>A
MANE Select
|
ENSP00000325527.5:p.Thr2297=
|
|
ENST00000674301.1:c.1995G>A
|
ENSP00000501333.1:n.1995G>A
|
|
ENST00000316623.9:c.6891G>A
|
ENSP00000325527.5:p.Thr2297=
|
|
ENST00000559133.5:c.2198G>A
|
|
|
ENST00000560720.1:n.178G>A
|
|
|
NM_000138.4:c.6891G>A , LRG_778t1:c.6891G>A
|
NP_000129.3:p.Thr2297=
|
|
NM_000138.5:c.6891G>A
MANE Select
|
NP_000129.3:p.Thr2297=
|
|