ENST00000695651.1:n.2095G>A
|
|
|
ENST00000695652.1:c.3624G>A
|
ENSP00000512083.1:p.Val1208=
|
|
ENST00000695653.1:c.1656G>A
|
ENSP00000512084.1:p.Val552=
|
|
ENST00000695654.1:c.2772G>A
|
ENSP00000512085.1:p.Val924=
|
|
ENST00000695655.1:c.2688G>A
|
ENSP00000512086.1:n.2688G>A
|
|
ENST00000695692.1:n.3111G>A
|
|
|
ENST00000245907.11:c.3747G>A
MANE Select
|
ENSP00000245907.4:p.Val1249=
|
|
ENST00000245907.10:c.3747G>A
|
ENSP00000245907.4:p.Val1249=
|
|
ENST00000596238.1:n.190G>A
|
|
|
ENST00000601008.1:c.241+559G>A
|
ENSP00000471384.1:n.241+559G>A
|
|
NM_000064.3:c.3747G>A
|
NP_000055.2:p.Val1249=
|
|
NM_000064.4:c.3747G>A
MANE Select
|
NP_000055.2:p.Val1249=
|
|