ENST00000559133.6:c.*1160T>G
|
ENSP00000453958.2:n.*1160T>G
|
|
ENST00000674301.2:c.*1865T>G
|
ENSP00000501333.2:n.*1865T>G
|
|
ENST00000682158.1:n.1733T>G
|
|
|
ENST00000682170.1:n.2533T>G
|
|
|
ENST00000682767.1:n.1649T>G
|
|
|
ENST00000316623.10:c.8352T>G
MANE Select
|
ENSP00000325527.5:p.Leu2784=
|
|
ENST00000674301.1:c.3518T>G
|
ENSP00000501333.1:n.3518T>G
|
|
ENST00000316623.9:c.8352T>G
|
ENSP00000325527.5:p.Leu2784=
|
|
ENST00000559133.5:c.3721T>G
|
|
|
ENST00000561429.1:n.607T>G
|
|
|
NM_000138.4:c.8352T>G , LRG_778t1:c.8352T>G
|
NP_000129.3:p.Leu2784=
|
|
NM_000138.5:c.8352T>G
MANE Select
|
NP_000129.3:p.Leu2784=
|
|