ENST00000695651.1:n.935A>G
|
|
|
ENST00000695652.1:c.2464A>G
|
ENSP00000512083.1:p.Arg822Gly
|
|
ENST00000695653.1:c.496A>G
|
ENSP00000512084.1:p.Arg166Gly
|
|
ENST00000695654.1:c.1711A>G
|
ENSP00000512085.1:p.Arg571Gly
|
|
ENST00000695655.1:c.1528A>G
|
ENSP00000512086.1:n.1528A>G
|
|
ENST00000695692.1:n.1951A>G
|
|
|
ENST00000245907.11:c.2587A>G
MANE Select
|
ENSP00000245907.4:p.Arg863Gly
|
|
ENST00000245907.10:c.2587A>G
|
ENSP00000245907.4:p.Arg863Gly
|
|
ENST00000594005.1:n.163A>G
|
|
|
NM_000064.3:c.2587A>G
|
NP_000055.2:p.Arg863Gly
|
|
NM_000064.4:c.2587A>G
MANE Select
|
NP_000055.2:p.Arg863Gly
|
|