ENST00000270357.10:c.1562C>G
MANE Select
|
ENSP00000270357.4:p.Pro521Arg
|
|
ENST00000270357.8:c.869C>G
|
ENSP00000270357.3:p.Pro290Arg
|
|
ENST00000437406.1:c.128C>G
|
ENSP00000403319.1:p.Pro43Arg
|
|
ENST00000451363.5:c.203C>G
|
ENSP00000414661.1:p.Pro68Arg
|
|
ENST00000464550.5:n.398C>G
|
|
|
ENST00000471657.1:n.365C>G
|
|
|
ENST00000481757.5:n.2496C>G
|
|
|
ENST00000486058.5:n.1675C>G
|
|
|
ENST00000493398.5:n.708C>G
|
|
|
NM_018226.4:c.1562C>G
|
NP_060696.4:p.Pro521Arg
|
|
XM_005247036.3:c.1529C>G
|
XP_005247093.1:p.Pro510Arg
|
|
NM_018226.5:c.1562C>G
|
NP_060696.4:p.Pro521Arg
|
|
XM_005247036.4:c.1529C>G
|
XP_005247093.1:p.Pro510Arg
|
|
NM_018226.6:c.1562C>G
MANE Select
|
NP_060696.4:p.Pro521Arg
|
|