ENST00000695651.1:n.1039A>G
|
|
|
ENST00000695652.1:c.2568A>G
|
ENSP00000512083.1:p.Pro856=
|
|
ENST00000695653.1:c.600A>G
|
ENSP00000512084.1:p.Pro200=
|
|
ENST00000695654.1:c.1815A>G
|
ENSP00000512085.1:p.Pro605=
|
|
ENST00000695655.1:c.1632A>G
|
ENSP00000512086.1:n.1632A>G
|
|
ENST00000695692.1:n.2055A>G
|
|
|
ENST00000245907.11:c.2691A>G
MANE Select
|
ENSP00000245907.4:p.Pro897=
|
|
ENST00000245907.10:c.2691A>G
|
ENSP00000245907.4:p.Pro897=
|
|
ENST00000594005.1:n.267A>G
|
|
|
NM_000064.3:c.2691A>G
|
NP_000055.2:p.Pro897=
|
|
NM_000064.4:c.2691A>G
MANE Select
|
NP_000055.2:p.Pro897=
|
|