ENST00000339157.10:c.1054C>T
MANE Select
|
ENSP00000341408.5:p.Arg352Ter
|
|
ENST00000376542.8:c.1054C>T
|
ENSP00000365725.3:p.Arg352Ter
|
|
ENST00000465694.2:c.508C>T
|
ENSP00000459278.2:p.Arg170Ter
|
|
ENST00000671784.1:c.429C>T
|
ENSP00000500451.1:p.Leu143=
|
|
ENST00000671858.1:c.508C>T
|
ENSP00000500550.1:p.Arg170Ter
|
|
ENST00000672114.1:c.483+1228C>T
|
ENSP00000499945.1:n.483+1228C>T
|
|
ENST00000672258.1:c.484-46C>T
|
ENSP00000499868.1:n.484-46C>T
|
|
ENST00000672331.1:c.425C>T
|
ENSP00000500286.1:n.425C>T
|
|
ENST00000672358.1:c.508C>T
|
ENSP00000500062.1:p.Arg170Ter
|
|
ENST00000672406.1:c.*393C>T
|
ENSP00000500208.1:n.*393C>T
|
|
ENST00000672566.1:c.583C>T
|
ENSP00000500106.1:p.Arg195Ter
|
|
ENST00000672596.1:c.508C>T
|
ENSP00000500290.1:p.Arg170Ter
|
|
ENST00000672871.1:c.404+4511C>T
|
ENSP00000499949.1:n.404+4511C>T
|
|
ENST00000673121.1:c.610C>T
|
ENSP00000499839.1:p.Arg204Ter
|
|
ENST00000673227.1:c.508C>T
|
ENSP00000500514.1:p.Arg170Ter
|
|
ENST00000673524.1:c.616C>T
|
|
|
ENST00000339157.9:c.1054C>T
|
ENSP00000341408.5:p.Arg352Ter
|
|
ENST00000376542.7:c.1054C>T
|
ENSP00000365725.3:p.Arg352Ter
|
|
NM_001042472.2:c.1054C>T
|
NP_001035937.1:p.Arg352Ter
|
|
NM_015600.4:c.1054C>T
|
NP_056415.1:p.Arg352Ter
|
|
XM_005260699.3:c.1029+1228C>T
|
XP_005260756.1:n.1029+1228C>T
|
|
XM_011529214.1:c.1054C>T
|
XP_011527516.1:p.Arg352Ter
|
|
XM_011529214.2:c.1054C>T
|
XP_011527516.1:p.Arg352Ter
|
|
XM_017027796.1:c.583C>T
|
XP_016883285.1:p.Arg195Ter
|
|
XR_002958465.1:n.2267C>T
|
|
|
XR_002958466.1:n.2387C>T
|
|
|
XR_002958467.1:n.1946C>T
|
|
|
NM_001042472.3:c.1054C>T
MANE Select
|
NP_001035937.1:p.Arg352Ter
|
|
NM_015600.5:c.1054C>T
|
NP_056415.1:p.Arg352Ter
|
|