ENST00000695651.1:n.913G>T
|
|
|
ENST00000695652.1:c.2442G>T
|
ENSP00000512083.1:p.Arg814=
|
|
ENST00000695653.1:c.474G>T
|
ENSP00000512084.1:p.Arg158=
|
|
ENST00000695654.1:c.1689G>T
|
ENSP00000512085.1:p.Arg563=
|
|
ENST00000695655.1:c.1506G>T
|
ENSP00000512086.1:n.1506G>T
|
|
ENST00000695692.1:n.1929G>T
|
|
|
ENST00000245907.11:c.2565G>T
MANE Select
|
ENSP00000245907.4:p.Arg855=
|
|
ENST00000245907.10:c.2565G>T
|
ENSP00000245907.4:p.Arg855=
|
|
ENST00000594005.1:n.46G>T
|
|
|
ENST00000602053.1:n.613G>T
|
|
|
NM_000064.3:c.2565G>T
|
NP_000055.2:p.Arg855=
|
|
NM_000064.4:c.2565G>T
MANE Select
|
NP_000055.2:p.Arg855=
|
|