ENST00000695651.1:n.810T>G
|
|
|
ENST00000695652.1:c.2339T>G
|
ENSP00000512083.1:p.Phe780Cys
|
|
ENST00000695653.1:c.371T>G
|
ENSP00000512084.1:p.Phe124Cys
|
|
ENST00000695654.1:c.1586T>G
|
ENSP00000512085.1:p.Phe529Cys
|
|
ENST00000695655.1:c.1403T>G
|
ENSP00000512086.1:n.1403T>G
|
|
ENST00000695692.1:n.1826T>G
|
|
|
ENST00000245907.11:c.2462T>G
MANE Select
|
ENSP00000245907.4:p.Phe821Cys
|
|
ENST00000245907.10:c.2462T>G
|
ENSP00000245907.4:p.Phe821Cys
|
|
ENST00000602053.1:n.510T>G
|
|
|
NM_000064.3:c.2462T>G
|
NP_000055.2:p.Phe821Cys
|
|
NM_000064.4:c.2462T>G
MANE Select
|
NP_000055.2:p.Phe821Cys
|
|