ENST00000695651.1:n.2091T>G
|
|
|
ENST00000695652.1:c.3620T>G
|
ENSP00000512083.1:p.Phe1207Cys
|
|
ENST00000695653.1:c.1652T>G
|
ENSP00000512084.1:p.Phe551Cys
|
|
ENST00000695654.1:c.2768T>G
|
ENSP00000512085.1:p.Phe923Cys
|
|
ENST00000695655.1:c.2684T>G
|
ENSP00000512086.1:n.2684T>G
|
|
ENST00000695692.1:n.3107T>G
|
|
|
ENST00000245907.11:c.3743T>G
MANE Select
|
ENSP00000245907.4:p.Phe1248Cys
|
|
ENST00000245907.10:c.3743T>G
|
ENSP00000245907.4:p.Phe1248Cys
|
|
ENST00000596238.1:n.186T>G
|
|
|
ENST00000601008.1:c.241+555T>G
|
ENSP00000471384.1:n.241+555T>G
|
|
NM_000064.3:c.3743T>G
|
NP_000055.2:p.Phe1248Cys
|
|
NM_000064.4:c.3743T>G
MANE Select
|
NP_000055.2:p.Phe1248Cys
|
|