ENST00000695901.1:c.799-768T>G
|
ENSP00000512251.1:n.799-768T>G
|
|
ENST00000695911.1:c.913T>G
|
ENSP00000512262.1:n.913T>G
|
|
ENST00000695912.1:c.1132T>G
|
ENSP00000512263.1:p.Cys378Gly
|
|
ENST00000695913.1:c.*1888T>G
|
ENSP00000512264.1:n.*1888T>G
|
|
ENST00000695914.1:c.895T>G
|
ENSP00000512265.1:p.Cys299Gly
|
|
ENST00000695918.1:n.363T>G
|
|
|
ENST00000306721.8:c.1135T>G
MANE Select
|
ENSP00000306968.3:p.Cys379Gly
|
|
ENST00000306721.7:c.1135T>G
|
ENSP00000306968.3:p.Cys379Gly
|
|
ENST00000347703.7:c.898T>G
|
ENSP00000272789.4:p.Cys300Gly
|
|
ENST00000410019.3:c.772T>G
|
ENSP00000386833.3:p.Cys258Gly
|
|
ENST00000410101.7:c.1003T>G
|
ENSP00000386656.3:p.Cys335Gly
|
|
ENST00000467411.5:n.1769-768T>G
|
|
|
ENST00000496441.5:n.1889T>G
|
|
|
NM_031942.4:c.1135T>G
|
NP_114148.3:p.Cys379Gly
|
|
NM_145810.2:c.898T>G
|
NP_665809.1:p.Cys300Gly
|
|
XM_011511957.1:c.1054T>G
|
XP_011510259.1:p.Cys352Gly
|
|
XR_923034.1:n.2033T>G
|
|
|
NM_031942.5:c.1135T>G
MANE Select
|
NP_114148.3:p.Cys379Gly
|
|
NM_145810.3:c.898T>G
|
NP_665809.1:p.Cys300Gly
|
|