ENST00000460680.6:c.2019G=
MANE Select
|
ENSP00000417132.1:p.Glu673=
|
|
ENST00000296288.9:c.1965G=
|
ENSP00000296288.5:p.Glu655=
|
|
ENST00000460680.5:c.2019G=
|
ENSP00000417132.1:p.Glu673=
|
|
ENST00000466093.1:n.692G=
|
|
|
ENST00000469613.5:c.218G=
|
|
|
ENST00000478368.1:c.591G=
|
ENSP00000420647.1:p.Glu197=
|
|
NM_004656.3:c.2019G=
|
NP_004647.1:p.Glu673=
|
|
XM_011534149.1:c.2088G=
|
XP_011532451.1:p.Glu696=
|
|
XM_011534150.1:c.2043G=
|
XP_011532452.1:p.Glu681=
|
|
XM_011534151.1:c.2034G=
|
XP_011532453.1:p.Glu678=
|
|
XM_011534152.1:c.1974G=
|
XP_011532454.1:p.Glu658=
|
|
XM_011534149.3:c.2088G=
|
XP_011532451.1:p.Glu696=
|
|
XM_011534150.3:c.2043G=
|
XP_011532452.1:p.Glu681=
|
|
XM_011534151.3:c.2034G=
|
XP_011532453.1:p.Glu678=
|
|
XM_011534152.2:c.1974G=
|
XP_011532454.1:p.Glu658=
|
|
XM_017007303.2:c.1965G=
|
XP_016862792.1:p.Glu655=
|
|
NM_004656.4:c.2019G=
MANE Select
|
NP_004647.1:p.Glu673=
|
|