ENST00000369762.7:c.972-7T=
MANE Select
|
ENSP00000358777.2:n.972-7T=
|
|
ENST00000439372.6:c.*934-7T=
|
ENSP00000408317.1:n.*934-7T=
|
|
ENST00000484908.2:n.1498-7T=
|
|
|
ENST00000619046.5:c.588-7T=
|
ENSP00000482243.2:n.588-7T=
|
|
ENST00000677332.1:c.907-7T=
|
ENSP00000502914.1:n.907-7T=
|
|
ENST00000677342.1:c.*250-7T=
|
ENSP00000503173.1:n.*250-7T=
|
|
ENST00000678317.1:n.1504-7T=
|
|
|
ENST00000679241.1:c.*38-7T=
|
ENSP00000503588.1:n.*38-7T=
|
|
ENST00000369762.6:c.972-7T=
|
ENSP00000358777.2:n.972-7T=
|
|
ENST00000422890.5:c.714-7T=
|
ENSP00000398511.1:n.714-7T=
|
|
ENST00000429585.5:c.664-7T=
|
ENSP00000408470.1:n.664-7T=
|
|
ENST00000455205.5:c.3450-7T=
|
|
|
ENST00000491569.5:n.1014-7T=
|
|
|
ENST00000619046.4:c.405-7T=
|
ENSP00000482243.1:n.405-7T=
|
|
NM_001183.5:c.972-7T=
|
NP_001174.2:n.972-7T=
|
|
XM_011531179.1:c.405-7T=
|
XP_011529481.1:n.405-7T=
|
|
NM_001183.6:c.972-7T=
MANE Select
|
NP_001174.2:n.972-7T=
|
|