ENST00000283249.7:c.898G>A
MANE Select
|
ENSP00000283249.2:p.Glu300Lys
|
|
ENST00000652612.1:n.341G>A
|
|
|
ENST00000283249.6:c.898G>A
|
ENSP00000283249.2:p.Glu300Lys
|
|
ENST00000409583.5:c.*512G>A
|
ENSP00000386477.1:n.*512G>A
|
|
ENST00000409872.1:c.898G>A
|
ENSP00000386367.1:p.Glu300Lys
|
|
ENST00000409967.6:c.898G>A
|
ENSP00000386828.2:p.Glu300Lys
|
|
ENST00000428609.6:c.772G>A
|
ENSP00000408024.2:p.Glu258Lys
|
|
ENST00000485635.1:n.1350G>A
|
|
|
ENST00000620391.4:c.613G>A
|
ENSP00000481183.1:p.Glu205Lys
|
|
NM_000888.4:c.898G>A
|
NP_000879.2:p.Glu300Lys
|
|
NM_001282353.1:c.898G>A
|
NP_001269282.1:p.Glu300Lys
|
|
NM_001282354.1:c.613G>A
|
NP_001269283.1:p.Glu205Lys
|
|
NM_001282355.1:c.898G>A
|
NP_001269284.1:p.Glu300Lys
|
|
NM_001282388.1:c.772G>A
|
NP_001269317.1:p.Glu258Lys
|
|
NM_001282389.1:c.679G>A
|
NP_001269318.1:p.Glu227Lys
|
|
NM_001282390.1:c.484G>A
|
NP_001269319.1:p.Glu162Lys
|
|
NM_000888.5:c.898G>A
MANE Select
|
NP_000879.2:p.Glu300Lys
|
|
NM_001282353.2:c.898G>A
|
NP_001269282.1:p.Glu300Lys
|
|
NM_001282355.2:c.898G>A
|
NP_001269284.1:p.Glu300Lys
|
|
NM_001282388.2:c.772G>A
|
NP_001269317.1:p.Glu258Lys
|
|
NM_001282389.2:c.679G>A
|
NP_001269318.1:p.Glu227Lys
|
|
NM_001282390.2:c.484G>A
|
NP_001269319.1:p.Glu162Lys
|
|
NM_001282354.2:c.613G>A
|
NP_001269283.1:p.Glu205Lys
|
|