ENST00000270357.10:c.1547C>A
MANE Select
|
ENSP00000270357.4:p.Pro516Gln
|
|
ENST00000270357.8:c.854C>A
|
ENSP00000270357.3:p.Pro285Gln
|
|
ENST00000437406.1:c.113C>A
|
ENSP00000403319.1:p.Pro38Gln
|
|
ENST00000451363.5:c.188C>A
|
ENSP00000414661.1:p.Pro63Gln
|
|
ENST00000464550.5:n.383C>A
|
|
|
ENST00000471657.1:n.350C>A
|
|
|
ENST00000481757.5:n.2481C>A
|
|
|
ENST00000486058.5:n.1660C>A
|
|
|
ENST00000493398.5:n.693C>A
|
|
|
NM_018226.4:c.1547C>A
|
NP_060696.4:p.Pro516Gln
|
|
XM_005247036.3:c.1514C>A
|
XP_005247093.1:p.Pro505Gln
|
|
NM_018226.5:c.1547C>A
|
NP_060696.4:p.Pro516Gln
|
|
XM_005247036.4:c.1514C>A
|
XP_005247093.1:p.Pro505Gln
|
|
NM_018226.6:c.1547C>A
MANE Select
|
NP_060696.4:p.Pro516Gln
|
|