ENST00000270357.10:c.1542A>G
MANE Select
|
ENSP00000270357.4:p.Thr514=
|
|
ENST00000270357.8:c.849A>G
|
ENSP00000270357.3:p.Thr283=
|
|
ENST00000437406.1:c.110-2A>G
|
ENSP00000403319.1:n.110-2A>G
|
|
ENST00000451363.5:c.183A>G
|
ENSP00000414661.1:p.Thr61=
|
|
ENST00000464550.5:n.378A>G
|
|
|
ENST00000471657.1:n.345A>G
|
|
|
ENST00000481757.5:n.2476A>G
|
|
|
ENST00000486058.5:n.1655A>G
|
|
|
ENST00000493398.5:n.688A>G
|
|
|
NM_018226.4:c.1542A>G
|
NP_060696.4:p.Thr514=
|
|
XM_005247036.3:c.1511-2A>G
|
XP_005247093.1:n.1511-2A>G
|
|
NM_018226.5:c.1542A>G
|
NP_060696.4:p.Thr514=
|
|
XM_005247036.4:c.1511-2A>G
|
XP_005247093.1:n.1511-2A>G
|
|
NM_018226.6:c.1542A>G
MANE Select
|
NP_060696.4:p.Thr514=
|
|