ENST00000695651.1:n.2046C>G
|
|
|
ENST00000695652.1:c.3575C>G
|
ENSP00000512083.1:p.Thr1192Arg
|
|
ENST00000695653.1:c.1607C>G
|
ENSP00000512084.1:p.Thr536Arg
|
|
ENST00000695654.1:c.2723C>G
|
ENSP00000512085.1:p.Thr908Arg
|
|
ENST00000695655.1:c.2639C>G
|
ENSP00000512086.1:n.2639C>G
|
|
ENST00000695692.1:n.3062C>G
|
|
|
ENST00000245907.11:c.3698C>G
MANE Select
|
ENSP00000245907.4:p.Thr1233Arg
|
|
ENST00000245907.10:c.3698C>G
|
ENSP00000245907.4:p.Thr1233Arg
|
|
ENST00000596238.1:n.141C>G
|
|
|
ENST00000601008.1:c.241+510C>G
|
ENSP00000471384.1:n.241+510C>G
|
|
NM_000064.3:c.3698C>G
|
NP_000055.2:p.Thr1233Arg
|
|
NM_000064.4:c.3698C>G
MANE Select
|
NP_000055.2:p.Thr1233Arg
|
|