ENST00000302328.9:c.2684A>T
MANE Select
|
ENSP00000307599.3:p.Glu895Val
|
|
ENST00000668754.1:c.2684A>T
|
ENSP00000499569.1:p.Glu895Val
|
|
ENST00000675223.1:c.2684A>T
|
ENSP00000502481.1:p.Glu895Val
|
|
ENST00000675672.1:c.2684A>T
|
ENSP00000502446.1:p.Glu895Val
|
|
ENST00000675892.1:c.2504A>T
|
ENSP00000502318.1:p.Glu835Val
|
|
ENST00000676045.1:c.2728A>T
|
ENSP00000501685.1:n.2728A>T
|
|
ENST00000676176.1:c.2303A>T
|
ENSP00000501891.1:p.Glu768Val
|
|
ENST00000302328.7:c.2684A>T
|
ENSP00000307599.3:p.Glu895Val
|
|
ENST00000444237.2:c.2684A>T
|
ENSP00000408028.2:p.Glu895Val
|
|
ENST00000456224.7:c.2684A>T
|
ENSP00000416757.3:p.Glu895Val
|
|
NM_001287223.1:c.2684A>T
|
NP_001274152.1:p.Glu895Val
|
|
NM_014139.2:c.2684A>T
|
NP_054858.2:p.Glu895Val
|
|
XM_011533320.1:c.2684A>T
|
XP_011531622.1:p.Glu895Val
|
|
XM_011533321.1:c.2021A>T
|
XP_011531623.1:p.Glu674Val
|
|
XM_011533322.1:c.1232A>T
|
XP_011531624.1:p.Glu411Val
|
|
NM_001349253.1:c.2684A>T
|
NP_001336182.1:p.Glu895Val
|
|
XM_011533321.2:c.2021A>T
|
XP_011531623.1:p.Glu674Val
|
|
XM_017005647.1:c.3059A>T
|
XP_016861136.1:p.Glu1020Val
|
|
XM_017005648.1:c.2486A>T
|
XP_016861137.1:p.Glu829Val
|
|
XM_017005650.1:c.2684A>T
|
XP_016861139.1:p.Glu895Val
|
|
XM_017005651.1:c.2411A>T
|
XP_016861140.1:p.Glu804Val
|
|
XM_017005652.1:c.2684A>T
|
XP_016861141.1:p.Glu895Val
|
|
XM_017005653.1:c.1088A>T
|
XP_016861142.1:p.Glu363Val
|
|
NM_001349253.2:c.2684A>T
MANE Select
|
NP_001336182.1:p.Glu895Val
|
|
NM_014139.3:c.2684A>T
|
NP_054858.2:p.Glu895Val
|
|