ENST00000691183.1:c.*251C>G
|
ENSP00000509954.1:n.*251C>G
|
|
ENST00000378842.8:c.663C>G
MANE Select
|
ENSP00000368119.4:p.Tyr221Ter
|
|
ENST00000378842.7:c.663C>G
|
ENSP00000368119.3:p.Tyr221Ter
|
|
ENST00000450095.6:c.336C>G
|
ENSP00000401956.2:p.Tyr112Ter
|
|
ENST00000472111.5:n.919C>G
|
|
|
ENST00000473506.6:c.*251C>G
|
ENSP00000432839.2:n.*251C>G
|
|
ENST00000473529.5:n.822C>G
|
|
|
ENST00000487381.5:n.1048C>G
|
|
|
ENST00000489643.6:n.438C>G
|
|
|
ENST00000554085.5:c.*407C>G
|
ENSP00000450419.1:n.*407C>G
|
|
ENST00000554550.5:c.*283C>G
|
ENSP00000451435.1:n.*283C>G
|
|
ENST00000554638.5:n.1135C>G
|
|
|
ENST00000555020.5:n.819C>G
|
|
|
ENST00000555086.5:n.667C>G
|
|
|
ENST00000555214.5:n.484C>G
|
|
|
ENST00000555754.1:n.8C>G
|
|
|
ENST00000556244.1:c.650C>G
|
|
|
ENST00000556278.1:c.408C>G
|
ENSP00000451792.1:p.Tyr136Ter
|
|
ENST00000556494.5:n.784C>G
|
|
|
ENST00000557706.5:n.1225C>G
|
|
|
NM_000155.3:c.663C>G
|
NP_000146.2:p.Tyr221Ter
|
|
NM_001258332.1:c.336C>G
|
NP_001245261.1:p.Tyr112Ter
|
|
NM_000155.4:c.663C>G
MANE Select
|
NP_000146.2:p.Tyr221Ter
|
|
NM_001258332.2:c.336C>G
|
NP_001245261.1:p.Tyr112Ter
|
|