ENST00000460680.6:c.2098C=
MANE Select
|
ENSP00000417132.1:p.Arg700=
|
|
ENST00000296288.9:c.2044C=
|
ENSP00000296288.5:p.Arg682=
|
|
ENST00000460680.5:c.2098C=
|
ENSP00000417132.1:p.Arg700=
|
|
ENST00000466093.1:n.771C=
|
|
|
ENST00000469613.5:c.297C=
|
|
|
ENST00000478368.1:c.670C=
|
ENSP00000420647.1:p.Arg224=
|
|
NM_004656.3:c.2098C=
|
NP_004647.1:p.Arg700=
|
|
XM_011534149.1:c.2167C=
|
XP_011532451.1:p.Arg723=
|
|
XM_011534150.1:c.2122C=
|
XP_011532452.1:p.Arg708=
|
|
XM_011534151.1:c.2113C=
|
XP_011532453.1:p.Arg705=
|
|
XM_011534152.1:c.2053C=
|
XP_011532454.1:p.Arg685=
|
|
XM_011534149.3:c.2167C=
|
XP_011532451.1:p.Arg723=
|
|
XM_011534150.3:c.2122C=
|
XP_011532452.1:p.Arg708=
|
|
XM_011534151.3:c.2113C=
|
XP_011532453.1:p.Arg705=
|
|
XM_011534152.2:c.2053C=
|
XP_011532454.1:p.Arg685=
|
|
XM_017007303.2:c.2044C=
|
XP_016862792.1:p.Arg682=
|
|
NM_004656.4:c.2098C=
MANE Select
|
NP_004647.1:p.Arg700=
|
|