ENST00000695651.1:n.2279A>G
|
|
|
ENST00000695653.1:c.1840A>G
|
ENSP00000512084.1:p.Ile614Val
|
|
ENST00000695654.1:c.2956A>G
|
ENSP00000512085.1:p.Ile986Val
|
|
ENST00000695690.1:n.122A>G
|
|
|
ENST00000695691.1:n.122A>G
|
|
|
ENST00000245907.11:c.3931A>G
MANE Select
|
ENSP00000245907.4:p.Ile1311Val
|
|
ENST00000245907.10:c.3931A>G
|
ENSP00000245907.4:p.Ile1311Val
|
|
ENST00000596238.1:n.374A>G
|
|
|
ENST00000596548.1:c.13A>G
|
ENSP00000469744.1:p.Ile5Val
|
|
ENST00000601008.1:c.241+1720A>G
|
ENSP00000471384.1:n.241+1720A>G
|
|
NM_000064.3:c.3931A>G
|
NP_000055.2:p.Ile1311Val
|
|
NM_000064.4:c.3931A>G
MANE Select
|
NP_000055.2:p.Ile1311Val
|
|