ENST00000695651.1:n.856C>A
|
|
|
ENST00000695652.1:c.2385C>A
|
ENSP00000512083.1:p.Pro795=
|
|
ENST00000695653.1:c.417C>A
|
ENSP00000512084.1:p.Pro139=
|
|
ENST00000695654.1:c.1632C>A
|
ENSP00000512085.1:p.Pro544=
|
|
ENST00000695655.1:c.1449C>A
|
ENSP00000512086.1:n.1449C>A
|
|
ENST00000695692.1:n.1872C>A
|
|
|
ENST00000245907.11:c.2508C>A
MANE Select
|
ENSP00000245907.4:p.Pro836=
|
|
ENST00000245907.10:c.2508C>A
|
ENSP00000245907.4:p.Pro836=
|
|
ENST00000602053.1:n.556C>A
|
|
|
NM_000064.3:c.2508C>A
|
NP_000055.2:p.Pro836=
|
|
NM_000064.4:c.2508C>A
MANE Select
|
NP_000055.2:p.Pro836=
|
|