ENST00000460680.6:c.2018A>T
MANE Select
|
ENSP00000417132.1:p.Glu673Val
|
|
ENST00000296288.9:c.1964A>T
|
ENSP00000296288.5:p.Glu655Val
|
|
ENST00000460680.5:c.2018A>T
|
ENSP00000417132.1:p.Glu673Val
|
|
ENST00000466093.1:n.691A>T
|
|
|
ENST00000469613.5:c.217A>T
|
|
|
ENST00000478368.1:c.590A>T
|
ENSP00000420647.1:p.Glu197Val
|
|
NM_004656.3:c.2018A>T
|
NP_004647.1:p.Glu673Val
|
|
XM_011534149.1:c.2087A>T
|
XP_011532451.1:p.Glu696Val
|
|
XM_011534150.1:c.2042A>T
|
XP_011532452.1:p.Glu681Val
|
|
XM_011534151.1:c.2033A>T
|
XP_011532453.1:p.Glu678Val
|
|
XM_011534152.1:c.1973A>T
|
XP_011532454.1:p.Glu658Val
|
|
XM_011534149.3:c.2087A>T
|
XP_011532451.1:p.Glu696Val
|
|
XM_011534150.3:c.2042A>T
|
XP_011532452.1:p.Glu681Val
|
|
XM_011534151.3:c.2033A>T
|
XP_011532453.1:p.Glu678Val
|
|
XM_011534152.2:c.1973A>T
|
XP_011532454.1:p.Glu658Val
|
|
XM_017007303.2:c.1964A>T
|
XP_016862792.1:p.Glu655Val
|
|
NM_004656.4:c.2018A>T
MANE Select
|
NP_004647.1:p.Glu673Val
|
|