ENST00000559133.6:c.*1217C>T
|
ENSP00000453958.2:n.*1217C>T
|
|
ENST00000674301.2:c.*1922C>T
|
ENSP00000501333.2:n.*1922C>T
|
|
ENST00000682158.1:n.1790C>T
|
|
|
ENST00000682170.1:n.2590C>T
|
|
|
ENST00000682767.1:n.1706C>T
|
|
|
ENST00000316623.10:c.8409C>T
MANE Select
|
ENSP00000325527.5:p.Phe2803=
|
|
ENST00000674301.1:c.3575C>T
|
ENSP00000501333.1:n.3575C>T
|
|
ENST00000316623.9:c.8409C>T
|
ENSP00000325527.5:p.Phe2803=
|
|
ENST00000559133.5:c.3778C>T
|
|
|
NM_000138.4:c.8409C>T , LRG_778t1:c.8409C>T
|
NP_000129.3:p.Phe2803=
|
|
NM_000138.5:c.8409C>T
MANE Select
|
NP_000129.3:p.Phe2803=
|
|