ENST00000695651.1:n.1123C>T
|
|
|
ENST00000695652.1:c.2652C>T
|
ENSP00000512083.1:p.Val884=
|
|
ENST00000695653.1:c.684C>T
|
ENSP00000512084.1:p.Val228=
|
|
ENST00000695654.1:c.1899C>T
|
ENSP00000512085.1:p.Val633=
|
|
ENST00000695655.1:c.1716C>T
|
ENSP00000512086.1:n.1716C>T
|
|
ENST00000695692.1:n.2139C>T
|
|
|
ENST00000245907.11:c.2775C>T
MANE Select
|
ENSP00000245907.4:p.Val925=
|
|
ENST00000245907.10:c.2775C>T
|
ENSP00000245907.4:p.Val925=
|
|
ENST00000594005.1:n.351C>T
|
|
|
NM_000064.3:c.2775C>T
|
NP_000055.2:p.Val925=
|
|
NM_000064.4:c.2775C>T
MANE Select
|
NP_000055.2:p.Val925=
|
|