ENST00000695651.1:n.1122T>G
|
|
|
ENST00000695652.1:c.2651T>G
|
ENSP00000512083.1:p.Val884Gly
|
|
ENST00000695653.1:c.683T>G
|
ENSP00000512084.1:p.Val228Gly
|
|
ENST00000695654.1:c.1898T>G
|
ENSP00000512085.1:p.Val633Gly
|
|
ENST00000695655.1:c.1715T>G
|
ENSP00000512086.1:n.1715T>G
|
|
ENST00000695692.1:n.2138T>G
|
|
|
ENST00000245907.11:c.2774T>G
MANE Select
|
ENSP00000245907.4:p.Val925Gly
|
|
ENST00000245907.10:c.2774T>G
|
ENSP00000245907.4:p.Val925Gly
|
|
ENST00000594005.1:n.350T>G
|
|
|
NM_000064.3:c.2774T>G
|
NP_000055.2:p.Val925Gly
|
|
NM_000064.4:c.2774T>G
MANE Select
|
NP_000055.2:p.Val925Gly
|
|