ENST00000559133.6:c.*1303G>T
|
ENSP00000453958.2:n.*1303G>T
|
|
ENST00000674301.2:c.*2008G>T
|
ENSP00000501333.2:n.*2008G>T
|
|
ENST00000682158.1:n.1876G>T
|
|
|
ENST00000682170.1:n.2676G>T
|
|
|
ENST00000682767.1:n.1792G>T
|
|
|
ENST00000316623.10:c.8495G>T
MANE Select
|
ENSP00000325527.5:p.Ser2832Ile
|
|
ENST00000674301.1:c.3661G>T
|
ENSP00000501333.1:n.3661G>T
|
|
ENST00000316623.9:c.8495G>T
|
ENSP00000325527.5:p.Ser2832Ile
|
|
ENST00000559133.5:c.3864G>T
|
|
|
NM_000138.4:c.8495G>T , LRG_778t1:c.8495G>T
|
NP_000129.3:p.Ser2832Ile
|
|
NM_000138.5:c.8495G>T
MANE Select
|
NP_000129.3:p.Ser2832Ile
|
|