ENST00000460680.6:c.544G>C
MANE Select
|
ENSP00000417132.1:p.Glu182Gln
|
|
ENST00000296288.9:c.544G>C
|
ENSP00000296288.5:p.Glu182Gln
|
|
ENST00000460680.5:c.544G>C
|
ENSP00000417132.1:p.Glu182Gln
|
|
ENST00000470173.1:c.307G>C
|
ENSP00000417776.1:p.Glu103Gln
|
|
ENST00000471532.5:n.259G>C
|
|
|
ENST00000483984.5:n.437+189G>C
|
|
|
ENST00000490917.1:c.*285G>C
|
ENSP00000419709.1:n.*285G>C
|
|
NM_004656.3:c.544G>C
|
NP_004647.1:p.Glu182Gln
|
|
XM_011534149.1:c.544G>C
|
XP_011532451.1:p.Glu182Gln
|
|
XM_011534150.1:c.544G>C
|
XP_011532452.1:p.Glu182Gln
|
|
XM_011534151.1:c.544G>C
|
XP_011532453.1:p.Glu182Gln
|
|
XM_011534152.1:c.544G>C
|
XP_011532454.1:p.Glu182Gln
|
|
XM_011534149.3:c.544G>C
|
XP_011532451.1:p.Glu182Gln
|
|
XM_011534150.3:c.544G>C
|
XP_011532452.1:p.Glu182Gln
|
|
XM_011534151.3:c.544G>C
|
XP_011532453.1:p.Glu182Gln
|
|
XM_011534152.2:c.544G>C
|
XP_011532454.1:p.Glu182Gln
|
|
XM_017007303.2:c.544G>C
|
XP_016862792.1:p.Glu182Gln
|
|
NM_004656.4:c.544G>C
MANE Select
|
NP_004647.1:p.Glu182Gln
|
|