ENST00000695651.1:n.850G>T
|
|
|
ENST00000695652.1:c.2379G>T
|
ENSP00000512083.1:p.Arg793=
|
|
ENST00000695653.1:c.411G>T
|
ENSP00000512084.1:p.Arg137=
|
|
ENST00000695654.1:c.1626G>T
|
ENSP00000512085.1:p.Arg542=
|
|
ENST00000695655.1:c.1443G>T
|
ENSP00000512086.1:n.1443G>T
|
|
ENST00000695692.1:n.1866G>T
|
|
|
ENST00000245907.11:c.2502G>T
MANE Select
|
ENSP00000245907.4:p.Arg834=
|
|
ENST00000245907.10:c.2502G>T
|
ENSP00000245907.4:p.Arg834=
|
|
ENST00000602053.1:n.550G>T
|
|
|
NM_000064.3:c.2502G>T
|
NP_000055.2:p.Arg834=
|
|
NM_000064.4:c.2502G>T
MANE Select
|
NP_000055.2:p.Arg834=
|
|