ENST00000330889.8:c.922G>T
MANE Select
|
ENSP00000329468.3:p.Glu308Ter
|
|
ENST00000330889.7:c.922G>T
|
ENSP00000329468.3:p.Glu308Ter
|
|
ENST00000470962.1:n.342G>T
|
|
|
ENST00000480980.1:n.356G>T
|
|
|
ENST00000580525.5:c.940G>T
|
ENSP00000464121.1:p.Glu314Ter
|
|
ENST00000581285.5:c.838G>T
|
ENSP00000464155.1:p.Glu280Ter
|
|
ENST00000584828.5:c.291G>T
|
|
|
ENST00000584989.1:c.214G>T
|
ENSP00000462634.1:p.Glu72Ter
|
|
ENST00000585130.5:c.*521G>T
|
ENSP00000464120.1:n.*521G>T
|
|
NM_018404.2:c.922G>T
|
NP_060874.1:p.Glu308Ter
|
|
XM_005258008.2:c.940G>T
|
XP_005258065.1:p.Glu314Ter
|
|
XM_005258011.2:c.877G>T
|
XP_005258068.1:p.Glu293Ter
|
|
XM_006721973.2:c.940G>T
|
XP_006722036.1:p.Glu314Ter
|
|
XM_011524993.1:c.937G>T
|
XP_011523295.1:p.Glu313Ter
|
|
XM_011524994.1:c.919G>T
|
XP_011523296.1:p.Glu307Ter
|
|
NM_001346712.1:c.940G>T
|
NP_001333641.1:p.Glu314Ter
|
|
NM_001346714.1:c.919G>T
|
NP_001333643.1:p.Glu307Ter
|
|
NM_001346716.1:c.922G>T
|
NP_001333645.1:p.Glu308Ter
|
|
NR_144488.1:n.1121G>T
|
|
|
XM_024450831.1:c.922G>T
|
XP_024306599.1:p.Glu308Ter
|
|
XM_024450832.1:c.937G>T
|
XP_024306600.1:p.Glu313Ter
|
|
XM_024450833.1:c.877G>T
|
XP_024306601.1:p.Glu293Ter
|
|
XM_024450834.1:c.940G>T
|
XP_024306602.1:p.Glu314Ter
|
|
XM_024450835.1:c.556G>T
|
XP_024306603.1:p.Glu186Ter
|
|
NM_018404.3:c.922G>T
MANE Select
|
NP_060874.1:p.Glu308Ter
|
|
NM_001346712.2:c.940G>T
|
NP_001333641.1:p.Glu314Ter
|
|
NM_001346714.2:c.919G>T
|
NP_001333643.1:p.Glu307Ter
|
|
NM_001346716.2:c.922G>T
|
NP_001333645.1:p.Glu308Ter
|
|
NR_144488.2:n.912G>T
|
|
|