ENST00000675785.2:c.1021G>T
|
ENSP00000502019.1:p.Glu341Ter
|
|
ENST00000373477.9:c.1168G>T
MANE Select
|
ENSP00000362576.4:p.Glu390Ter
|
|
ENST00000674629.1:c.*716G>T
|
ENSP00000502470.1:n.*716G>T
|
|
ENST00000674654.1:c.*1128G>T
|
ENSP00000501729.1:n.*1128G>T
|
|
ENST00000675785.1:c.1021G>T
|
ENSP00000502019.1:p.Glu341Ter
|
|
ENST00000676297.1:c.*1342G>T
|
ENSP00000501596.1:n.*1342G>T
|
|
ENST00000373477.8:c.1168G>T
|
ENSP00000362576.4:p.Glu390Ter
|
|
ENST00000469100.5:n.1084G>T
|
|
|
ENST00000478828.1:n.635G>T
|
|
|
ENST00000487404.5:n.1478G>T
|
|
|
ENST00000490826.1:n.461G>T
|
|
|
ENST00000616261.1:c.1167G>T
|
ENSP00000484192.1:p.Ter389Tyr
|
|
NM_003680.3:c.1168G>T , LRG_273t1:c.1168G>T
|
NP_003671.1:p.Glu390Ter
|
|
XM_011542347.1:c.538G>T
|
XP_011540649.1:p.Glu180Ter
|
|
XM_011542348.1:c.538G>T
|
XP_011540650.1:p.Glu180Ter
|
|
XM_011542347.2:c.538G>T
|
XP_011540649.1:p.Glu180Ter
|
|
XM_017002651.2:c.538G>T
|
XP_016858140.1:p.Glu180Ter
|
|
NM_003680.4:c.1168G>T
MANE Select
|
NP_003671.1:p.Glu390Ter
|
|