ENST00000559133.6:c.*1034+91G>A
|
ENSP00000453958.2:n.*1034+91G>A
|
|
ENST00000674301.2:c.*1739+91G>A
|
ENSP00000501333.2:n.*1739+91G>A
|
|
ENST00000682158.1:n.1607+91G>A
|
|
|
ENST00000682170.1:n.2407+91G>A
|
|
|
ENST00000682767.1:n.1523+91G>A
|
|
|
ENST00000316623.10:c.8226+91G>A
MANE Select
|
ENSP00000325527.5:n.8226+91G>A
|
|
ENST00000674301.1:c.3392+91G>A
|
ENSP00000501333.1:n.3392+91G>A
|
|
ENST00000316623.9:c.8226+91G>A
|
ENSP00000325527.5:n.8226+91G>A
|
|
ENST00000559133.5:c.3595+91G>A
|
|
|
ENST00000561429.1:n.481+91G>A
|
|
|
NM_000138.4:c.8226+91G>A , LRG_778t1:c.8226+91G>A
|
NP_000129.3:n.8226+91G>A
|
|
NM_000138.5:c.8226+91G>A
MANE Select
|
NP_000129.3:n.8226+91G>A
|
|