ENST00000695651.1:n.2003C>G
|
|
|
ENST00000695652.1:c.3532C>G
|
ENSP00000512083.1:p.Arg1178Gly
|
|
ENST00000695653.1:c.1564C>G
|
ENSP00000512084.1:p.Arg522Gly
|
|
ENST00000695654.1:c.2680C>G
|
ENSP00000512085.1:p.Arg894Gly
|
|
ENST00000695655.1:c.2596C>G
|
ENSP00000512086.1:n.2596C>G
|
|
ENST00000695692.1:n.3019C>G
|
|
|
ENST00000245907.11:c.3655C>G
MANE Select
|
ENSP00000245907.4:p.Arg1219Gly
|
|
ENST00000245907.10:c.3655C>G
|
ENSP00000245907.4:p.Arg1219Gly
|
|
ENST00000596238.1:n.98C>G
|
|
|
ENST00000601008.1:c.241+467C>G
|
ENSP00000471384.1:n.241+467C>G
|
|
NM_000064.3:c.3655C>G
|
NP_000055.2:p.Arg1219Gly
|
|
NM_000064.4:c.3655C>G
MANE Select
|
NP_000055.2:p.Arg1219Gly
|
|