ENST00000460680.6:c.2026T=
MANE Select
|
ENSP00000417132.1:p.Cys676=
|
|
ENST00000296288.9:c.1972T=
|
ENSP00000296288.5:p.Cys658=
|
|
ENST00000460680.5:c.2026T=
|
ENSP00000417132.1:p.Cys676=
|
|
ENST00000466093.1:n.699T=
|
|
|
ENST00000469613.5:c.225T=
|
|
|
ENST00000478368.1:c.598T=
|
ENSP00000420647.1:p.Cys200=
|
|
NM_004656.3:c.2026T=
|
NP_004647.1:p.Cys676=
|
|
XM_011534149.1:c.2095T=
|
XP_011532451.1:p.Cys699=
|
|
XM_011534150.1:c.2050T=
|
XP_011532452.1:p.Cys684=
|
|
XM_011534151.1:c.2041T=
|
XP_011532453.1:p.Cys681=
|
|
XM_011534152.1:c.1981T=
|
XP_011532454.1:p.Cys661=
|
|
XM_011534149.3:c.2095T=
|
XP_011532451.1:p.Cys699=
|
|
XM_011534150.3:c.2050T=
|
XP_011532452.1:p.Cys684=
|
|
XM_011534151.3:c.2041T=
|
XP_011532453.1:p.Cys681=
|
|
XM_011534152.2:c.1981T=
|
XP_011532454.1:p.Cys661=
|
|
XM_017007303.2:c.1972T=
|
XP_016862792.1:p.Cys658=
|
|
NM_004656.4:c.2026T=
MANE Select
|
NP_004647.1:p.Cys676=
|
|