ENST00000559133.6:c.*1096T>G
|
ENSP00000453958.2:n.*1096T>G
|
|
ENST00000674301.2:c.*1801T>G
|
ENSP00000501333.2:n.*1801T>G
|
|
ENST00000682158.1:n.1669T>G
|
|
|
ENST00000682170.1:n.2469T>G
|
|
|
ENST00000682767.1:n.1585T>G
|
|
|
ENST00000316623.10:c.8288T>G
MANE Select
|
ENSP00000325527.5:p.Ile2763Ser
|
|
ENST00000674301.1:c.3454T>G
|
ENSP00000501333.1:n.3454T>G
|
|
ENST00000316623.9:c.8288T>G
|
ENSP00000325527.5:p.Ile2763Ser
|
|
ENST00000559133.5:c.3657T>G
|
|
|
ENST00000561429.1:n.543T>G
|
|
|
NM_000138.4:c.8288T>G , LRG_778t1:c.8288T>G
|
NP_000129.3:p.Ile2763Ser
|
|
NM_000138.5:c.8288T>G
MANE Select
|
NP_000129.3:p.Ile2763Ser
|
|