ENST00000559133.6:c.*419T>G
|
ENSP00000453958.2:n.*419T>G
|
|
ENST00000674301.2:c.*1124T>G
|
ENSP00000501333.2:n.*1124T>G
|
|
ENST00000682170.1:n.1792T>G
|
|
|
ENST00000682767.1:n.908T>G
|
|
|
ENST00000316623.10:c.7611T>G
MANE Select
|
ENSP00000325527.5:p.Ser2537=
|
|
ENST00000674301.1:c.2777T>G
|
ENSP00000501333.1:n.2777T>G
|
|
ENST00000316623.9:c.7611T>G
|
ENSP00000325527.5:p.Ser2537=
|
|
ENST00000559133.5:c.2980T>G
|
|
|
NM_000138.4:c.7611T>G , LRG_778t1:c.7611T>G
|
NP_000129.3:p.Ser2537=
|
|
NM_000138.5:c.7611T>G
MANE Select
|
NP_000129.3:p.Ser2537=
|
|