ENST00000695651.1:n.1041A>C
|
|
|
ENST00000695652.1:c.2570A>C
|
ENSP00000512083.1:p.Tyr857Ser
|
|
ENST00000695653.1:c.602A>C
|
ENSP00000512084.1:p.Tyr201Ser
|
|
ENST00000695654.1:c.1817A>C
|
ENSP00000512085.1:p.Tyr606Ser
|
|
ENST00000695655.1:c.1634A>C
|
ENSP00000512086.1:n.1634A>C
|
|
ENST00000695692.1:n.2057A>C
|
|
|
ENST00000245907.11:c.2693A>C
MANE Select
|
ENSP00000245907.4:p.Tyr898Ser
|
|
ENST00000245907.10:c.2693A>C
|
ENSP00000245907.4:p.Tyr898Ser
|
|
ENST00000594005.1:n.269A>C
|
|
|
NM_000064.3:c.2693A>C
|
NP_000055.2:p.Tyr898Ser
|
|
NM_000064.4:c.2693A>C
MANE Select
|
NP_000055.2:p.Tyr898Ser
|
|