ENST00000695651.1:n.1070C>T
|
|
|
ENST00000695652.1:c.2599C>T
|
ENSP00000512083.1:p.Gln867Ter
|
|
ENST00000695653.1:c.631C>T
|
ENSP00000512084.1:p.Gln211Ter
|
|
ENST00000695654.1:c.1846C>T
|
ENSP00000512085.1:p.Gln616Ter
|
|
ENST00000695655.1:c.1663C>T
|
ENSP00000512086.1:n.1663C>T
|
|
ENST00000695692.1:n.2086C>T
|
|
|
ENST00000245907.11:c.2722C>T
MANE Select
|
ENSP00000245907.4:p.Gln908Ter
|
|
ENST00000245907.10:c.2722C>T
|
ENSP00000245907.4:p.Gln908Ter
|
|
ENST00000594005.1:n.298C>T
|
|
|
NM_000064.3:c.2722C>T
|
NP_000055.2:p.Gln908Ter
|
|
NM_000064.4:c.2722C>T
MANE Select
|
NP_000055.2:p.Gln908Ter
|
|