ENST00000270357.10:c.1636G>T
MANE Select
|
ENSP00000270357.4:p.Asp546Tyr
|
|
ENST00000270357.8:c.943G>T
|
ENSP00000270357.3:p.Asp315Tyr
|
|
ENST00000437406.1:c.202G>T
|
ENSP00000403319.1:p.Asp68Tyr
|
|
ENST00000451363.5:c.277G>T
|
ENSP00000414661.1:p.Asp93Tyr
|
|
ENST00000464550.5:n.472G>T
|
|
|
ENST00000471657.1:n.439G>T
|
|
|
ENST00000481757.5:n.2570G>T
|
|
|
ENST00000486058.5:n.1749G>T
|
|
|
ENST00000493398.5:n.782G>T
|
|
|
NM_018226.4:c.1636G>T
|
NP_060696.4:p.Asp546Tyr
|
|
XM_005247036.3:c.1603G>T
|
XP_005247093.1:p.Asp535Tyr
|
|
NM_018226.5:c.1636G>T
|
NP_060696.4:p.Asp546Tyr
|
|
XM_005247036.4:c.1603G>T
|
XP_005247093.1:p.Asp535Tyr
|
|
NM_018226.6:c.1636G>T
MANE Select
|
NP_060696.4:p.Asp546Tyr
|
|