ENST00000695651.1:n.886A>C
|
|
|
ENST00000695652.1:c.2415A>C
|
ENSP00000512083.1:p.Glu805Asp
|
|
ENST00000695653.1:c.447A>C
|
ENSP00000512084.1:p.Glu149Asp
|
|
ENST00000695654.1:c.1662A>C
|
ENSP00000512085.1:p.Glu554Asp
|
|
ENST00000695655.1:c.1479A>C
|
ENSP00000512086.1:n.1479A>C
|
|
ENST00000695692.1:n.1902A>C
|
|
|
ENST00000245907.11:c.2538A>C
MANE Select
|
ENSP00000245907.4:p.Glu846Asp
|
|
ENST00000245907.10:c.2538A>C
|
ENSP00000245907.4:p.Glu846Asp
|
|
ENST00000594005.1:n.19A>C
|
|
|
ENST00000602053.1:n.586A>C
|
|
|
NM_000064.3:c.2538A>C
|
NP_000055.2:p.Glu846Asp
|
|
NM_000064.4:c.2538A>C
MANE Select
|
NP_000055.2:p.Glu846Asp
|
|