ENST00000675785.2:c.1045G>T
|
ENSP00000502019.1:p.Glu349Ter
|
|
ENST00000373477.9:c.1192G>T
MANE Select
|
ENSP00000362576.4:p.Glu398Ter
|
|
ENST00000674629.1:c.*740G>T
|
ENSP00000502470.1:n.*740G>T
|
|
ENST00000674654.1:c.*1152G>T
|
ENSP00000501729.1:n.*1152G>T
|
|
ENST00000675785.1:c.1045G>T
|
ENSP00000502019.1:p.Glu349Ter
|
|
ENST00000676297.1:c.*1366G>T
|
ENSP00000501596.1:n.*1366G>T
|
|
ENST00000373477.8:c.1192G>T
|
ENSP00000362576.4:p.Glu398Ter
|
|
ENST00000469100.5:n.1108G>T
|
|
|
ENST00000478828.1:n.659G>T
|
|
|
ENST00000487404.5:n.1502G>T
|
|
|
ENST00000490826.1:n.485G>T
|
|
|
NM_003680.3:c.1192G>T , LRG_273t1:c.1192G>T
|
NP_003671.1:p.Glu398Ter
|
|
XM_011542347.1:c.562G>T
|
XP_011540649.1:p.Glu188Ter
|
|
XM_011542348.1:c.562G>T
|
XP_011540650.1:p.Glu188Ter
|
|
XM_011542347.2:c.562G>T
|
XP_011540649.1:p.Glu188Ter
|
|
XM_017002651.2:c.562G>T
|
XP_016858140.1:p.Glu188Ter
|
|
NM_003680.4:c.1192G>T
MANE Select
|
NP_003671.1:p.Glu398Ter
|
|