ENST00000695651.1:n.1102T>G
|
|
|
ENST00000695652.1:c.2631T>G
|
ENSP00000512083.1:p.His877Gln
|
|
ENST00000695653.1:c.663T>G
|
ENSP00000512084.1:p.His221Gln
|
|
ENST00000695654.1:c.1878T>G
|
ENSP00000512085.1:p.His626Gln
|
|
ENST00000695655.1:c.1695T>G
|
ENSP00000512086.1:n.1695T>G
|
|
ENST00000695692.1:n.2118T>G
|
|
|
ENST00000245907.11:c.2754T>G
MANE Select
|
ENSP00000245907.4:p.His918Gln
|
|
ENST00000245907.10:c.2754T>G
|
ENSP00000245907.4:p.His918Gln
|
|
ENST00000594005.1:n.330T>G
|
|
|
NM_000064.3:c.2754T>G
|
NP_000055.2:p.His918Gln
|
|
NM_000064.4:c.2754T>G
MANE Select
|
NP_000055.2:p.His918Gln
|
|