ENST00000695651.1:n.2072C>A
|
|
|
ENST00000695652.1:c.3601C>A
|
ENSP00000512083.1:p.Gln1201Lys
|
|
ENST00000695653.1:c.1633C>A
|
ENSP00000512084.1:p.Gln545Lys
|
|
ENST00000695654.1:c.2749C>A
|
ENSP00000512085.1:p.Gln917Lys
|
|
ENST00000695655.1:c.2665C>A
|
ENSP00000512086.1:n.2665C>A
|
|
ENST00000695692.1:n.3088C>A
|
|
|
ENST00000245907.11:c.3724C>A
MANE Select
|
ENSP00000245907.4:p.Gln1242Lys
|
|
ENST00000245907.10:c.3724C>A
|
ENSP00000245907.4:p.Gln1242Lys
|
|
ENST00000596238.1:n.167C>A
|
|
|
ENST00000601008.1:c.241+536C>A
|
ENSP00000471384.1:n.241+536C>A
|
|
NM_000064.3:c.3724C>A
|
NP_000055.2:p.Gln1242Lys
|
|
NM_000064.4:c.3724C>A
MANE Select
|
NP_000055.2:p.Gln1242Lys
|
|