ENST00000695651.1:n.979C>G
|
|
|
ENST00000695652.1:c.2508C>G
|
ENSP00000512083.1:p.Thr836=
|
|
ENST00000695653.1:c.540C>G
|
ENSP00000512084.1:p.Thr180=
|
|
ENST00000695654.1:c.1755C>G
|
ENSP00000512085.1:p.Thr585=
|
|
ENST00000695655.1:c.1572C>G
|
ENSP00000512086.1:n.1572C>G
|
|
ENST00000695692.1:n.1995C>G
|
|
|
ENST00000245907.11:c.2631C>G
MANE Select
|
ENSP00000245907.4:p.Thr877=
|
|
ENST00000245907.10:c.2631C>G
|
ENSP00000245907.4:p.Thr877=
|
|
ENST00000594005.1:n.207C>G
|
|
|
NM_000064.3:c.2631C>G
|
NP_000055.2:p.Thr877=
|
|
NM_000064.4:c.2631C>G
MANE Select
|
NP_000055.2:p.Thr877=
|
|