ENST00000559133.6:c.*262-299G>T
|
ENSP00000453958.2:n.*262-299G>T
|
|
ENST00000674301.2:c.*967-299G>T
|
ENSP00000501333.2:n.*967-299G>T
|
|
ENST00000682170.1:n.1635-299G>T
|
|
|
ENST00000682767.1:n.751-299G>T
|
|
|
ENST00000316623.10:c.7454-299G>T
MANE Select
|
ENSP00000325527.5:n.7454-299G>T
|
|
ENST00000674301.1:c.2620-299G>T
|
ENSP00000501333.1:n.2620-299G>T
|
|
ENST00000316623.9:c.7454-299G>T
|
ENSP00000325527.5:n.7454-299G>T
|
|
ENST00000559133.5:c.2823-299G>T
|
|
|
NM_000138.4:c.7454-299G>T , LRG_778t1:c.7454-299G>T
|
NP_000129.3:n.7454-299G>T
|
|
NM_000138.5:c.7454-299G>T
MANE Select
|
NP_000129.3:n.7454-299G>T
|
|