ENST00000270357.10:c.1533C>T
MANE Select
|
ENSP00000270357.4:p.Leu511=
|
|
ENST00000270357.8:c.840C>T
|
ENSP00000270357.3:p.Leu280=
|
|
ENST00000437406.1:c.110-11C>T
|
ENSP00000403319.1:n.110-11C>T
|
|
ENST00000451363.5:c.174C>T
|
ENSP00000414661.1:p.Leu58=
|
|
ENST00000464550.5:n.369C>T
|
|
|
ENST00000471657.1:n.336C>T
|
|
|
ENST00000481757.5:n.2467C>T
|
|
|
ENST00000486058.5:n.1646C>T
|
|
|
ENST00000493398.5:n.679C>T
|
|
|
NM_018226.4:c.1533C>T
|
NP_060696.4:p.Leu511=
|
|
XM_005247036.3:c.1511-11C>T
|
XP_005247093.1:n.1511-11C>T
|
|
NM_018226.5:c.1533C>T
|
NP_060696.4:p.Leu511=
|
|
XM_005247036.4:c.1511-11C>T
|
XP_005247093.1:n.1511-11C>T
|
|
NM_018226.6:c.1533C>T
MANE Select
|
NP_060696.4:p.Leu511=
|
|