ENST00000442544.7:c.2428G=
MANE Select
|
ENSP00000389140.2:p.Glu810=
|
|
ENST00000304775.12:c.2229G=
|
|
|
ENST00000412726.5:c.2359G=
|
ENSP00000397322.2:p.Glu787=
|
|
ENST00000442544.6:c.2428G=
|
ENSP00000389140.2:p.Glu810=
|
|
ENST00000581580.5:c.1393G=
|
ENSP00000464582.1:p.Glu465=
|
|
NM_005215.3:c.2428G=
|
NP_005206.2:p.Glu810=
|
|
XM_011525843.1:c.2428G=
|
XP_011524145.1:p.Glu810=
|
|
XM_011525844.1:c.1393G=
|
XP_011524146.1:p.Glu465=
|
|
XM_011525845.1:c.2428G=
|
XP_011524147.1:p.Glu810=
|
|
XM_011525846.1:c.2428G=
|
XP_011524148.1:p.Glu810=
|
|
XM_011525844.2:c.1393G=
|
XP_011524146.1:p.Glu465=
|
|
XM_017025568.1:c.2428G=
|
XP_016881057.1:p.Glu810=
|
|
XM_017025569.1:c.2428G=
|
XP_016881058.1:p.Glu810=
|
|
XM_017025570.1:c.1393G=
|
XP_016881059.1:p.Glu465=
|
|
NM_005215.4:c.2428G=
MANE Select
|
NP_005206.2:p.Glu810=
|
|