ENST00000559133.6:c.*369T>G
|
ENSP00000453958.2:n.*369T>G
|
|
ENST00000674301.2:c.*1074T>G
|
ENSP00000501333.2:n.*1074T>G
|
|
ENST00000682170.1:n.1742T>G
|
|
|
ENST00000682767.1:n.858T>G
|
|
|
ENST00000316623.10:c.7561T>G
MANE Select
|
ENSP00000325527.5:p.Ser2521Ala
|
|
ENST00000674301.1:c.2727T>G
|
ENSP00000501333.1:n.2727T>G
|
|
ENST00000316623.9:c.7561T>G
|
ENSP00000325527.5:p.Ser2521Ala
|
|
ENST00000559133.5:c.2930T>G
|
|
|
NM_000138.4:c.7561T>G , LRG_778t1:c.7561T>G
|
NP_000129.3:p.Ser2521Ala
|
|
NM_000138.5:c.7561T>G
MANE Select
|
NP_000129.3:p.Ser2521Ala
|
|