ENST00000270357.10:c.1628A>C
MANE Select
|
ENSP00000270357.4:p.Glu543Ala
|
|
ENST00000270357.8:c.935A>C
|
ENSP00000270357.3:p.Glu312Ala
|
|
ENST00000437406.1:c.194A>C
|
ENSP00000403319.1:p.Glu65Ala
|
|
ENST00000451363.5:c.269A>C
|
ENSP00000414661.1:p.Glu90Ala
|
|
ENST00000464550.5:n.464A>C
|
|
|
ENST00000471657.1:n.431A>C
|
|
|
ENST00000481757.5:n.2562A>C
|
|
|
ENST00000486058.5:n.1741A>C
|
|
|
ENST00000493398.5:n.774A>C
|
|
|
NM_018226.4:c.1628A>C
|
NP_060696.4:p.Glu543Ala
|
|
XM_005247036.3:c.1595A>C
|
XP_005247093.1:p.Glu532Ala
|
|
NM_018226.5:c.1628A>C
|
NP_060696.4:p.Glu543Ala
|
|
XM_005247036.4:c.1595A>C
|
XP_005247093.1:p.Glu532Ala
|
|
NM_018226.6:c.1628A>C
MANE Select
|
NP_060696.4:p.Glu543Ala
|
|