ENST00000695651.1:n.2867C>G
|
|
|
ENST00000695653.1:c.2428C>G
|
ENSP00000512084.1:p.Arg810Gly
|
|
ENST00000695654.1:c.3544C>G
|
ENSP00000512085.1:p.Arg1182Gly
|
|
ENST00000695689.1:c.490C>G
|
ENSP00000512101.1:n.490C>G
|
|
ENST00000695690.1:n.1584C>G
|
|
|
ENST00000695691.1:n.1380C>G
|
|
|
ENST00000245907.11:c.4519C>G
MANE Select
|
ENSP00000245907.4:p.Arg1507Gly
|
|
ENST00000245907.10:c.4519C>G
|
ENSP00000245907.4:p.Arg1507Gly
|
|
ENST00000599668.1:n.114C>G
|
|
|
ENST00000599899.5:n.1478C>G
|
|
|
ENST00000601008.1:c.242-1476C>G
|
ENSP00000471384.1:n.242-1476C>G
|
|
NM_000064.3:c.4519C>G
|
NP_000055.2:p.Arg1507Gly
|
|
NM_000064.4:c.4519C>G
MANE Select
|
NP_000055.2:p.Arg1507Gly
|
|