ENST00000695651.1:n.816T>G
|
|
|
ENST00000695652.1:c.2345T>G
|
ENSP00000512083.1:p.Val782Gly
|
|
ENST00000695653.1:c.377T>G
|
ENSP00000512084.1:p.Val126Gly
|
|
ENST00000695654.1:c.1592T>G
|
ENSP00000512085.1:p.Val531Gly
|
|
ENST00000695655.1:c.1409T>G
|
ENSP00000512086.1:n.1409T>G
|
|
ENST00000695692.1:n.1832T>G
|
|
|
ENST00000245907.11:c.2468T>G
MANE Select
|
ENSP00000245907.4:p.Val823Gly
|
|
ENST00000245907.10:c.2468T>G
|
ENSP00000245907.4:p.Val823Gly
|
|
ENST00000602053.1:n.516T>G
|
|
|
NM_000064.3:c.2468T>G
|
NP_000055.2:p.Val823Gly
|
|
NM_000064.4:c.2468T>G
MANE Select
|
NP_000055.2:p.Val823Gly
|
|