ENST00000695651.1:n.991T>G
|
|
|
ENST00000695652.1:c.2520T>G
|
ENSP00000512083.1:p.Arg840=
|
|
ENST00000695653.1:c.552T>G
|
ENSP00000512084.1:p.Arg184=
|
|
ENST00000695654.1:c.1767T>G
|
ENSP00000512085.1:p.Arg589=
|
|
ENST00000695655.1:c.1584T>G
|
ENSP00000512086.1:n.1584T>G
|
|
ENST00000695692.1:n.2007T>G
|
|
|
ENST00000245907.11:c.2643T>G
MANE Select
|
ENSP00000245907.4:p.Arg881=
|
|
ENST00000245907.10:c.2643T>G
|
ENSP00000245907.4:p.Arg881=
|
|
ENST00000594005.1:n.219T>G
|
|
|
NM_000064.3:c.2643T>G
|
NP_000055.2:p.Arg881=
|
|
NM_000064.4:c.2643T>G
MANE Select
|
NP_000055.2:p.Arg881=
|
|