ENST00000270357.10:c.1547C>G
MANE Select
|
ENSP00000270357.4:p.Pro516Arg
|
|
ENST00000270357.8:c.854C>G
|
ENSP00000270357.3:p.Pro285Arg
|
|
ENST00000437406.1:c.113C>G
|
ENSP00000403319.1:p.Pro38Arg
|
|
ENST00000451363.5:c.188C>G
|
ENSP00000414661.1:p.Pro63Arg
|
|
ENST00000464550.5:n.383C>G
|
|
|
ENST00000471657.1:n.350C>G
|
|
|
ENST00000481757.5:n.2481C>G
|
|
|
ENST00000486058.5:n.1660C>G
|
|
|
ENST00000493398.5:n.693C>G
|
|
|
NM_018226.4:c.1547C>G
|
NP_060696.4:p.Pro516Arg
|
|
XM_005247036.3:c.1514C>G
|
XP_005247093.1:p.Pro505Arg
|
|
NM_018226.5:c.1547C>G
|
NP_060696.4:p.Pro516Arg
|
|
XM_005247036.4:c.1514C>G
|
XP_005247093.1:p.Pro505Arg
|
|
NM_018226.6:c.1547C>G
MANE Select
|
NP_060696.4:p.Pro516Arg
|
|