ENST00000270357.10:c.1567C>T
MANE Select
|
ENSP00000270357.4:p.Leu523=
|
|
ENST00000270357.8:c.874C>T
|
ENSP00000270357.3:p.Leu292=
|
|
ENST00000437406.1:c.133C>T
|
ENSP00000403319.1:p.Leu45=
|
|
ENST00000451363.5:c.208C>T
|
ENSP00000414661.1:p.Leu70=
|
|
ENST00000464550.5:n.403C>T
|
|
|
ENST00000471657.1:n.370C>T
|
|
|
ENST00000481757.5:n.2501C>T
|
|
|
ENST00000486058.5:n.1680C>T
|
|
|
ENST00000493398.5:n.713C>T
|
|
|
NM_018226.4:c.1567C>T
|
NP_060696.4:p.Leu523=
|
|
XM_005247036.3:c.1534C>T
|
XP_005247093.1:p.Leu512=
|
|
NM_018226.5:c.1567C>T
|
NP_060696.4:p.Leu523=
|
|
XM_005247036.4:c.1534C>T
|
XP_005247093.1:p.Leu512=
|
|
NM_018226.6:c.1567C>T
MANE Select
|
NP_060696.4:p.Leu523=
|
|