ENST00000456935.7:c.2856G=
MANE Select
|
ENSP00000395473.2:p.Gln952=
|
|
ENST00000221363.8:c.2853G=
|
ENSP00000221363.4:p.Gln951=
|
|
ENST00000456935.6:c.2856G=
|
ENSP00000395473.2:p.Gln952=
|
|
ENST00000466794.5:n.3446G=
|
|
|
ENST00000469423.1:n.285G=
|
|
|
ENST00000493218.5:n.267G=
|
|
|
ENST00000597692.1:c.415G=
|
|
|
NM_000528.3:c.2856G=
|
NP_000519.2:p.Gln952=
|
|
NM_001173498.1:c.2853G=
|
NP_001166969.1:p.Gln951=
|
|
XM_005259913.1:c.2859G=
|
XP_005259970.1:p.Gln953=
|
|
XM_011528017.1:c.1755G=
|
XP_011526319.1:p.Gln585=
|
|
XM_005259913.2:c.2859G=
|
XP_005259970.1:p.Gln953=
|
|
XM_024451518.1:c.1755G=
|
XP_024307286.1:p.Gln585=
|
|
NM_000528.4:c.2856G=
MANE Select
|
NP_000519.2:p.Gln952=
|
|
NM_001173498.2:c.2853G=
|
NP_001166969.1:p.Gln951=
|
|