ENST00000270357.10:c.1516G>T
MANE Select
|
ENSP00000270357.4:p.Glu506Ter
|
|
ENST00000270357.8:c.823G>T
|
ENSP00000270357.3:p.Glu275Ter
|
|
ENST00000437406.1:c.110-28G>T
|
ENSP00000403319.1:n.110-28G>T
|
|
ENST00000451363.5:c.157G>T
|
ENSP00000414661.1:p.Glu53Ter
|
|
ENST00000464550.5:n.352G>T
|
|
|
ENST00000471657.1:n.319G>T
|
|
|
ENST00000481757.5:n.2450G>T
|
|
|
ENST00000486058.5:n.1629G>T
|
|
|
ENST00000493398.5:n.662G>T
|
|
|
NM_018226.4:c.1516G>T
|
NP_060696.4:p.Glu506Ter
|
|
XM_005247036.3:c.1511-28G>T
|
XP_005247093.1:n.1511-28G>T
|
|
NM_018226.5:c.1516G>T
|
NP_060696.4:p.Glu506Ter
|
|
XM_005247036.4:c.1511-28G>T
|
XP_005247093.1:n.1511-28G>T
|
|
NM_018226.6:c.1516G>T
MANE Select
|
NP_060696.4:p.Glu506Ter
|
|