ENST00000470918.2:n.4629T>G
|
|
|
ENST00000695970.1:c.3427T>G
|
ENSP00000512297.1:p.Cys1143Gly
|
|
ENST00000695971.1:c.3580T>G
|
ENSP00000512298.1:p.Cys1194Gly
|
|
ENST00000695972.1:c.*678T>G
|
ENSP00000512299.1:n.*678T>G
|
|
ENST00000695973.1:c.*1965T>G
|
ENSP00000512300.1:n.*1965T>G
|
|
ENST00000695974.1:c.3424T>G
|
ENSP00000512301.1:p.Cys1142Gly
|
|
ENST00000695975.1:c.*1728T>G
|
ENSP00000512302.1:n.*1728T>G
|
|
ENST00000695976.1:c.3412T>G
|
ENSP00000512303.1:p.Cys1138Gly
|
|
ENST00000695981.1:c.3580+21T>G
|
ENSP00000512306.1:n.3580+21T>G
|
|
ENST00000695984.1:c.1609T>G
|
ENSP00000512309.1:p.Cys537Gly
|
|
ENST00000695986.1:c.*3252T>G
|
ENSP00000512311.1:n.*3252T>G
|
|
ENST00000695990.1:n.635T>G
|
|
|
ENST00000696026.1:c.*1883T>G
|
ENSP00000512335.1:n.*1883T>G
|
|
ENST00000696027.1:c.3595T>G
|
ENSP00000512336.1:p.Cys1199Gly
|
|
ENST00000696028.1:c.3529T>G
|
ENSP00000512337.1:p.Cys1177Gly
|
|
ENST00000696029.1:c.3595T>G
|
ENSP00000512338.1:p.Cys1199Gly
|
|
ENST00000696031.1:c.*3119T>G
|
ENSP00000512340.1:n.*3119T>G
|
|
ENST00000696032.1:c.3580+21T>G
|
ENSP00000512341.1:n.3580+21T>G
|
|
ENST00000696033.1:c.1160-32579T>G
|
ENSP00000512342.1:n.1160-32579T>G
|
|
ENST00000367429.9:c.3601T>G
MANE Select
|
ENSP00000356399.4:p.Cys1201Gly
|
|
ENST00000367429.8:c.3601T>G
|
ENSP00000356399.4:p.Cys1201Gly
|
|
ENST00000466229.5:n.6699T>G
|
|
|
NM_000186.3:c.3601T>G , LRG_47t1:c.3601T>G
|
NP_000177.2:p.Cys1201Gly
|
|
XR_001737134.2:n.3787T>G
|
|
|
NM_000186.4:c.3601T>G
MANE Select
|
NP_000177.2:p.Cys1201Gly
|
|