ENST00000559133.6:c.*1106C>G
|
ENSP00000453958.2:n.*1106C>G
|
|
ENST00000674301.2:c.*1811C>G
|
ENSP00000501333.2:n.*1811C>G
|
|
ENST00000682158.1:n.1679C>G
|
|
|
ENST00000682170.1:n.2479C>G
|
|
|
ENST00000682767.1:n.1595C>G
|
|
|
ENST00000316623.10:c.8298C>G
MANE Select
|
ENSP00000325527.5:p.Phe2766Leu
|
|
ENST00000674301.1:c.3464C>G
|
ENSP00000501333.1:n.3464C>G
|
|
ENST00000316623.9:c.8298C>G
|
ENSP00000325527.5:p.Phe2766Leu
|
|
ENST00000559133.5:c.3667C>G
|
|
|
ENST00000561429.1:n.553C>G
|
|
|
NM_000138.4:c.8298C>G , LRG_778t1:c.8298C>G
|
NP_000129.3:p.Phe2766Leu
|
|
NM_000138.5:c.8298C>G
MANE Select
|
NP_000129.3:p.Phe2766Leu
|
|