ENST00000695651.1:n.2032C>A
|
|
|
ENST00000695652.1:c.3561C>A
|
ENSP00000512083.1:p.Tyr1187Ter
|
|
ENST00000695653.1:c.1593C>A
|
ENSP00000512084.1:p.Tyr531Ter
|
|
ENST00000695654.1:c.2709C>A
|
ENSP00000512085.1:p.Tyr903Ter
|
|
ENST00000695655.1:c.2625C>A
|
ENSP00000512086.1:n.2625C>A
|
|
ENST00000695692.1:n.3048C>A
|
|
|
ENST00000245907.11:c.3684C>A
MANE Select
|
ENSP00000245907.4:p.Tyr1228Ter
|
|
ENST00000245907.10:c.3684C>A
|
ENSP00000245907.4:p.Tyr1228Ter
|
|
ENST00000596238.1:n.127C>A
|
|
|
ENST00000601008.1:c.241+496C>A
|
ENSP00000471384.1:n.241+496C>A
|
|
NM_000064.3:c.3684C>A
|
NP_000055.2:p.Tyr1228Ter
|
|
NM_000064.4:c.3684C>A
MANE Select
|
NP_000055.2:p.Tyr1228Ter
|
|