ENST00000695651.1:n.905A>T
|
|
|
ENST00000695652.1:c.2434A>T
|
ENSP00000512083.1:p.Asn812Tyr
|
|
ENST00000695653.1:c.466A>T
|
ENSP00000512084.1:p.Asn156Tyr
|
|
ENST00000695654.1:c.1681A>T
|
ENSP00000512085.1:p.Asn561Tyr
|
|
ENST00000695655.1:c.1498A>T
|
ENSP00000512086.1:n.1498A>T
|
|
ENST00000695692.1:n.1921A>T
|
|
|
ENST00000245907.11:c.2557A>T
MANE Select
|
ENSP00000245907.4:p.Asn853Tyr
|
|
ENST00000245907.10:c.2557A>T
|
ENSP00000245907.4:p.Asn853Tyr
|
|
ENST00000594005.1:n.38A>T
|
|
|
ENST00000602053.1:n.605A>T
|
|
|
NM_000064.3:c.2557A>T
|
NP_000055.2:p.Asn853Tyr
|
|
NM_000064.4:c.2557A>T
MANE Select
|
NP_000055.2:p.Asn853Tyr
|
|