ENST00000381129.8:c.955G>C
MANE Select
|
ENSP00000370521.3:p.Glu319Gln
|
|
ENST00000250087.9:c.766G>C
|
ENSP00000250087.5:p.Glu256Gln
|
|
ENST00000381128.2:c.*827G>C
|
ENSP00000370520.2:n.*827G>C
|
|
ENST00000381129.7:c.955G>C
|
ENSP00000370521.3:p.Glu319Gln
|
|
ENST00000570466.5:c.889G>C
|
ENSP00000461287.1:p.Glu297Gln
|
|
ENST00000570584.5:c.251+8259G>C
|
|
|
ENST00000574506.5:c.919G>C
|
ENSP00000458456.1:p.Glu307Gln
|
|
ENST00000575265.5:c.*926G>C
|
ENSP00000459673.1:n.*926G>C
|
|
ENST00000576307.5:c.775G>C
|
ENSP00000459522.1:p.Glu259Gln
|
|
ENST00000576776.5:c.883G>C
|
ENSP00000460827.1:p.Glu295Gln
|
|
ENST00000621374.4:c.954G>C
|
ENSP00000481337.1:p.Arg318Ser
|
|
NM_001033054.2:c.766G>C
|
NP_001028226.1:p.Glu256Gln
|
|
NM_001033055.2:c.775G>C
|
NP_001028227.1:p.Glu259Gln
|
|
NM_001285399.2:c.919G>C
|
NP_001272328.1:p.Glu307Gln
|
|
NM_001285400.2:c.889G>C
|
NP_001272329.1:p.Glu297Gln
|
|
NM_001285401.2:c.883G>C
|
NP_001272330.1:p.Glu295Gln
|
|
NM_001285402.1:c.838G>C
|
NP_001272331.1:p.Glu280Gln
|
|
NM_014336.4:c.955G>C
|
NP_055151.3:p.Glu319Gln
|
|
NM_001033054.3:c.766G>C
|
NP_001028226.1:p.Glu256Gln
|
|
NM_001033055.3:c.775G>C
|
NP_001028227.1:p.Glu259Gln
|
|
NM_001285399.3:c.919G>C
|
NP_001272328.1:p.Glu307Gln
|
|
NM_001285400.3:c.889G>C
|
NP_001272329.1:p.Glu297Gln
|
|
NM_001285401.3:c.883G>C
|
NP_001272330.1:p.Glu295Gln
|
|
NM_001285402.2:c.838G>C
|
NP_001272331.1:p.Glu280Gln
|
|
NM_001285403.3:c.*926G>C
|
NP_001272332.1:n.*926G>C
|
|
NM_014336.5:c.955G>C
MANE Select
|
NP_055151.3:p.Glu319Gln
|
|
NM_001285403.4:c.*926G>C
|
NP_001272332.1:n.*926G>C
|
|