ENST00000338034.9:c.2340G>A
MANE Select
|
ENSP00000337445.4:p.Glu780=
|
|
ENST00000338034.8:c.2340G>A
|
ENSP00000337445.4:p.Glu780=
|
|
ENST00000395962.6:c.2283G>A
|
ENSP00000379291.1:p.Glu761=
|
|
ENST00000426905.7:c.2220G>A
|
ENSP00000405223.3:p.Glu740=
|
|
ENST00000465825.5:n.2227G>A
|
|
|
ENST00000480891.5:n.2169G>A
|
|
|
ENST00000484122.5:n.3170G>A
|
|
|
ENST00000487229.6:n.1886G>A
|
|
|
ENST00000584650.5:c.1739G>A
|
|
|
NM_001165962.1:c.2220G>A
|
NP_001159434.1:p.Glu740=
|
|
NM_018127.6:c.2340G>A
|
NP_060597.4:p.Glu780=
|
|
NM_173717.1:c.2337G>A
|
NP_776065.1:p.Glu779=
|
|
XM_024450850.1:c.2499G>A
|
XP_024306618.1:p.Glu833=
|
|
XM_024450851.1:c.2421G>A
|
XP_024306619.1:p.Glu807=
|
|
XM_024450852.1:c.2418G>A
|
XP_024306620.1:p.Glu806=
|
|
XM_024450853.1:c.2415G>A
|
XP_024306621.1:p.Glu805=
|
|
XM_024450854.1:c.2379G>A
|
XP_024306622.1:p.Glu793=
|
|
XM_024450855.1:c.2298G>A
|
XP_024306623.1:p.Glu766=
|
|
XM_024450856.1:c.2217G>A
|
XP_024306624.1:p.Glu739=
|
|
XM_024450857.1:c.2217G>A
|
XP_024306625.1:p.Glu739=
|
|
XM_024450858.1:c.2136G>A
|
XP_024306626.1:p.Glu712=
|
|
XM_024450859.1:c.2133G>A
|
XP_024306627.1:p.Glu711=
|
|
XM_024450860.1:c.2058G>A
|
XP_024306628.1:p.Glu686=
|
|
XM_024450861.1:c.2058G>A
|
XP_024306629.1:p.Glu686=
|
|
XM_024450862.1:c.2055G>A
|
XP_024306630.1:p.Glu685=
|
|
NM_018127.7:c.2340G>A
MANE Select
|
NP_060597.4:p.Glu780=
|
|
NM_001165962.2:c.2220G>A
|
NP_001159434.1:p.Glu740=
|
|
NM_173717.2:c.2337G>A
|
NP_776065.1:p.Glu779=
|
|