ENST00000320694.13:c.769C>T
|
ENSP00000323512.8:p.Arg257Ter
|
|
ENST00000336483.10:c.859C>T
|
ENSP00000338554.5:p.Arg287Ter
|
|
ENST00000517643.2:c.1669C>T
|
ENSP00000513333.1:p.Arg557Ter
|
|
ENST00000517698.6:c.*639C>T
|
ENSP00000430424.1:n.*639C>T
|
|
ENST00000521657.6:c.1669C>T
|
ENSP00000429277.1:p.Arg557Ter
|
|
ENST00000522084.6:c.859C>T
|
ENSP00000429766.2:p.Arg287Ter
|
|
ENST00000697457.1:c.1594C>T
|
ENSP00000513315.1:p.Arg532Ter
|
|
ENST00000697458.1:c.1669C>T
|
ENSP00000513316.1:p.Arg557Ter
|
|
ENST00000697460.1:c.1144C>T
|
ENSP00000513318.1:p.Arg382Ter
|
|
ENST00000697461.1:c.1669C>T
|
ENSP00000513319.1:p.Arg557Ter
|
|
ENST00000697462.1:c.859C>T
|
ENSP00000513320.1:p.Arg287Ter
|
|
ENST00000697463.1:n.1310C>T
|
|
|
ENST00000697464.1:c.*635C>T
|
ENSP00000513322.1:n.*635C>T
|
|
ENST00000697465.1:c.706C>T
|
ENSP00000513323.1:p.Arg236Ter
|
|
ENST00000697466.1:c.676C>T
|
ENSP00000513324.1:p.Arg226Ter
|
|
ENST00000697467.1:c.580C>T
|
ENSP00000513325.1:p.Arg194Ter
|
|
ENST00000697468.1:c.652C>T
|
ENSP00000513326.1:p.Arg218Ter
|
|
ENST00000697469.1:c.361C>T
|
ENSP00000513327.1:p.Arg121Ter
|
|
ENST00000697470.1:c.265C>T
|
ENSP00000513328.1:p.Arg89Ter
|
|
ENST00000697557.1:c.652C>T
|
ENSP00000513335.1:p.Arg218Ter
|
|
ENST00000521381.6:c.1669C>T
MANE Select
|
ENSP00000428056.1:p.Arg557Ter
|
|
ENST00000320694.12:c.769C>T
|
ENSP00000323512.8:p.Arg257Ter
|
|
ENST00000336483.9:c.859C>T
|
ENSP00000338554.5:p.Arg287Ter
|
|
ENST00000517698.5:c.*639C>T
|
ENSP00000430424.1:n.*639C>T
|
|
ENST00000518813.5:n.2212C>T
|
|
|
ENST00000520550.1:n.1068C>T
|
|
|
ENST00000521381.5:c.1669C>T
|
ENSP00000428056.1:p.Arg557Ter
|
|
ENST00000521657.5:c.1669C>T
|
ENSP00000429277.1:p.Arg557Ter
|
|
ENST00000523872.1:c.580C>T
|
ENSP00000430098.1:p.Arg194Ter
|
|
NM_001242466.1:c.580C>T
|
NP_001229395.1:p.Arg194Ter
|
|
NM_181504.3:c.859C>T
|
NP_852556.2:p.Arg287Ter
|
|
NM_181523.2:c.1669C>T
|
NP_852664.1:p.Arg557Ter
|
|
NM_181524.1:c.769C>T
|
NP_852665.1:p.Arg257Ter
|
|
XM_005248542.2:c.1669C>T
|
XP_005248599.1:p.Arg557Ter
|
|
XM_011543493.1:c.1342C>T
|
XP_011541795.1:p.Arg448Ter
|
|
XM_005248542.3:c.1669C>T
|
XP_005248599.1:p.Arg557Ter
|
|
XM_011543493.3:c.1342C>T
|
XP_011541795.1:p.Arg448Ter
|
|
XM_017009585.2:c.1669C>T
|
XP_016865074.1:p.Arg557Ter
|
|
XM_017009586.1:c.1396C>T
|
XP_016865075.1:p.Arg466Ter
|
|
NM_181523.3:c.1669C>T
MANE Select
|
NP_852664.1:p.Arg557Ter
|
|
NM_001242466.2:c.580C>T
|
NP_001229395.1:p.Arg194Ter
|
|
NM_181504.4:c.859C>T
|
NP_852556.2:p.Arg287Ter
|
|
NM_181524.2:c.769C>T
|
NP_852665.1:p.Arg257Ter
|
|