ENST00000559133.6:c.*1114C>T
|
ENSP00000453958.2:n.*1114C>T
|
|
ENST00000674301.2:c.*1819C>T
|
ENSP00000501333.2:n.*1819C>T
|
|
ENST00000682158.1:n.1687C>T
|
|
|
ENST00000682170.1:n.2487C>T
|
|
|
ENST00000682767.1:n.1603C>T
|
|
|
ENST00000316623.10:c.8306C>T
MANE Select
|
ENSP00000325527.5:p.Ser2769Phe
|
|
ENST00000674301.1:c.3472C>T
|
ENSP00000501333.1:n.3472C>T
|
|
ENST00000316623.9:c.8306C>T
|
ENSP00000325527.5:p.Ser2769Phe
|
|
ENST00000559133.5:c.3675C>T
|
|
|
ENST00000561429.1:n.561C>T
|
|
|
NM_000138.4:c.8306C>T , LRG_778t1:c.8306C>T
|
NP_000129.3:p.Ser2769Phe
|
|
NM_000138.5:c.8306C>T
MANE Select
|
NP_000129.3:p.Ser2769Phe
|
|