ENST00000695651.1:n.880G=
|
|
|
ENST00000695652.1:c.2409G=
|
ENSP00000512083.1:p.Gln803=
|
|
ENST00000695653.1:c.441G=
|
ENSP00000512084.1:p.Gln147=
|
|
ENST00000695654.1:c.1656G=
|
ENSP00000512085.1:p.Gln552=
|
|
ENST00000695655.1:c.1473G=
|
ENSP00000512086.1:n.1473G=
|
|
ENST00000695692.1:n.1896G=
|
|
|
ENST00000245907.11:c.2532G=
MANE Select
|
ENSP00000245907.4:p.Gln844=
|
|
ENST00000245907.10:c.2532G=
|
ENSP00000245907.4:p.Gln844=
|
|
ENST00000594005.1:n.13G=
|
|
|
ENST00000602053.1:n.580G=
|
|
|
NM_000064.3:c.2532G=
|
NP_000055.2:p.Gln844=
|
|
NM_000064.4:c.2532G=
MANE Select
|
NP_000055.2:p.Gln844=
|
|