ENST00000302328.9:c.2674G>T
MANE Select
|
ENSP00000307599.3:p.Glu892Ter
|
|
ENST00000668754.1:c.2674G>T
|
ENSP00000499569.1:p.Glu892Ter
|
|
ENST00000675223.1:c.2674G>T
|
ENSP00000502481.1:p.Glu892Ter
|
|
ENST00000675672.1:c.2674G>T
|
ENSP00000502446.1:p.Glu892Ter
|
|
ENST00000675892.1:c.2494G>T
|
ENSP00000502318.1:p.Glu832Ter
|
|
ENST00000676045.1:c.2718G>T
|
ENSP00000501685.1:n.2718G>T
|
|
ENST00000676176.1:c.2293G>T
|
ENSP00000501891.1:p.Glu765Ter
|
|
ENST00000302328.7:c.2674G>T
|
ENSP00000307599.3:p.Glu892Ter
|
|
ENST00000444237.2:c.2674G>T
|
ENSP00000408028.2:p.Glu892Ter
|
|
ENST00000456224.7:c.2674G>T
|
ENSP00000416757.3:p.Glu892Ter
|
|
NM_001287223.1:c.2674G>T
|
NP_001274152.1:p.Glu892Ter
|
|
NM_014139.2:c.2674G>T
|
NP_054858.2:p.Glu892Ter
|
|
XM_011533320.1:c.2674G>T
|
XP_011531622.1:p.Glu892Ter
|
|
XM_011533321.1:c.2011G>T
|
XP_011531623.1:p.Glu671Ter
|
|
XM_011533322.1:c.1222G>T
|
XP_011531624.1:p.Glu408Ter
|
|
NM_001349253.1:c.2674G>T
|
NP_001336182.1:p.Glu892Ter
|
|
XM_011533321.2:c.2011G>T
|
XP_011531623.1:p.Glu671Ter
|
|
XM_017005647.1:c.3049G>T
|
XP_016861136.1:p.Glu1017Ter
|
|
XM_017005648.1:c.2476G>T
|
XP_016861137.1:p.Glu826Ter
|
|
XM_017005650.1:c.2674G>T
|
XP_016861139.1:p.Glu892Ter
|
|
XM_017005651.1:c.2401G>T
|
XP_016861140.1:p.Glu801Ter
|
|
XM_017005652.1:c.2674G>T
|
XP_016861141.1:p.Glu892Ter
|
|
XM_017005653.1:c.1078G>T
|
XP_016861142.1:p.Glu360Ter
|
|
NM_001349253.2:c.2674G>T
MANE Select
|
NP_001336182.1:p.Glu892Ter
|
|
NM_014139.3:c.2674G>T
|
NP_054858.2:p.Glu892Ter
|
|