ENST00000695651.1:n.1050T>G
|
|
|
ENST00000695652.1:c.2579T>G
|
ENSP00000512083.1:p.Val860Gly
|
|
ENST00000695653.1:c.611T>G
|
ENSP00000512084.1:p.Val204Gly
|
|
ENST00000695654.1:c.1826T>G
|
ENSP00000512085.1:p.Val609Gly
|
|
ENST00000695655.1:c.1643T>G
|
ENSP00000512086.1:n.1643T>G
|
|
ENST00000695692.1:n.2066T>G
|
|
|
ENST00000245907.11:c.2702T>G
MANE Select
|
ENSP00000245907.4:p.Val901Gly
|
|
ENST00000245907.10:c.2702T>G
|
ENSP00000245907.4:p.Val901Gly
|
|
ENST00000594005.1:n.278T>G
|
|
|
NM_000064.3:c.2702T>G
|
NP_000055.2:p.Val901Gly
|
|
NM_000064.4:c.2702T>G
MANE Select
|
NP_000055.2:p.Val901Gly
|
|