ENST00000695651.1:n.1124A>G
|
|
|
ENST00000695652.1:c.2653A>G
|
ENSP00000512083.1:p.Arg885Gly
|
|
ENST00000695653.1:c.685A>G
|
ENSP00000512084.1:p.Arg229Gly
|
|
ENST00000695654.1:c.1900A>G
|
ENSP00000512085.1:p.Arg634Gly
|
|
ENST00000695655.1:c.1717A>G
|
ENSP00000512086.1:n.1717A>G
|
|
ENST00000695692.1:n.2140A>G
|
|
|
ENST00000245907.11:c.2776A>G
MANE Select
|
ENSP00000245907.4:p.Arg926Gly
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|
ENST00000245907.10:c.2776A>G
|
ENSP00000245907.4:p.Arg926Gly
|
|
ENST00000594005.1:n.352A>G
|
|
|
NM_000064.3:c.2776A>G
|
NP_000055.2:p.Arg926Gly
|
|
NM_000064.4:c.2776A>G
MANE Select
|
NP_000055.2:p.Arg926Gly
|
|