ENST00000695651.1:n.884G>T
|
|
|
ENST00000695652.1:c.2413G>T
|
ENSP00000512083.1:p.Glu805Ter
|
|
ENST00000695653.1:c.445G>T
|
ENSP00000512084.1:p.Glu149Ter
|
|
ENST00000695654.1:c.1660G>T
|
ENSP00000512085.1:p.Glu554Ter
|
|
ENST00000695655.1:c.1477G>T
|
ENSP00000512086.1:n.1477G>T
|
|
ENST00000695692.1:n.1900G>T
|
|
|
ENST00000245907.11:c.2536G>T
MANE Select
|
ENSP00000245907.4:p.Glu846Ter
|
|
ENST00000245907.10:c.2536G>T
|
ENSP00000245907.4:p.Glu846Ter
|
|
ENST00000594005.1:n.17G>T
|
|
|
ENST00000602053.1:n.584G>T
|
|
|
NM_000064.3:c.2536G>T
|
NP_000055.2:p.Glu846Ter
|
|
NM_000064.4:c.2536G>T
MANE Select
|
NP_000055.2:p.Glu846Ter
|
|