ENST00000559133.6:c.6966T>C
|
ENSP00000453958.2:p.Phe2322=
|
|
ENST00000674301.2:c.*417T>C
|
ENSP00000501333.2:n.*417T>C
|
|
ENST00000682170.1:n.575T>C
|
|
|
ENST00000682767.1:n.201T>C
|
|
|
ENST00000316623.10:c.6966T>C
MANE Select
|
ENSP00000325527.5:p.Phe2322=
|
|
ENST00000674301.1:c.2070T>C
|
ENSP00000501333.1:n.2070T>C
|
|
ENST00000316623.9:c.6966T>C
|
ENSP00000325527.5:p.Phe2322=
|
|
ENST00000559133.5:c.2273T>C
|
|
|
ENST00000560720.1:n.253T>C
|
|
|
NM_000138.4:c.6966T>C , LRG_778t1:c.6966T>C
|
NP_000129.3:p.Phe2322=
|
|
NM_000138.5:c.6966T>C
MANE Select
|
NP_000129.3:p.Phe2322=
|
|