ENST00000695651.1:n.1083T>G
|
|
|
ENST00000695652.1:c.2612T>G
|
ENSP00000512083.1:p.Val871Gly
|
|
ENST00000695653.1:c.644T>G
|
ENSP00000512084.1:p.Val215Gly
|
|
ENST00000695654.1:c.1859T>G
|
ENSP00000512085.1:p.Val620Gly
|
|
ENST00000695655.1:c.1676T>G
|
ENSP00000512086.1:n.1676T>G
|
|
ENST00000695692.1:n.2099T>G
|
|
|
ENST00000245907.11:c.2735T>G
MANE Select
|
ENSP00000245907.4:p.Val912Gly
|
|
ENST00000245907.10:c.2735T>G
|
ENSP00000245907.4:p.Val912Gly
|
|
ENST00000594005.1:n.311T>G
|
|
|
NM_000064.3:c.2735T>G
|
NP_000055.2:p.Val912Gly
|
|
NM_000064.4:c.2735T>G
MANE Select
|
NP_000055.2:p.Val912Gly
|
|