|
NM_000138.5:c.7693T>C
MANE Select
|
NP_000129.3:p.Cys2565Arg
|
|
ENST00000316623.10:c.7693T>C
MANE Select
|
ENSP00000325527.5:p.Cys2565Arg
|
|
NM_000138.4:c.7693T>C , LRG_778t1:c.7693T>C
|
NP_000129.3:p.Cys2565Arg
|
|
ENST00000316623.9:c.7693T>C
|
ENSP00000325527.5:p.Cys2565Arg
|
|
ENST00000559133.5:c.3062T>C
|
|
|
ENST00000559133.6:c.*501T>C
|
ENSP00000453958.2:n.*501T>C
|
|
ENST00000674301.1:c.2859T>C
|
ENSP00000501333.1:n.2859T>C
|
|
ENST00000674301.2:c.*1206T>C
|
ENSP00000501333.2:n.*1206T>C
|
|
ENST00000682170.1:n.1874T>C
|
|
|
ENST00000682767.1:n.990T>C
|
|