ENST00000470918.2:n.4710T>G
|
|
|
ENST00000695970.1:c.3508T>G
|
ENSP00000512297.1:p.Cys1170Gly
|
|
ENST00000695971.1:c.3661T>G
|
ENSP00000512298.1:p.Cys1221Gly
|
|
ENST00000695972.1:c.*759T>G
|
ENSP00000512299.1:n.*759T>G
|
|
ENST00000695973.1:c.*2046T>G
|
ENSP00000512300.1:n.*2046T>G
|
|
ENST00000695974.1:c.3505T>G
|
ENSP00000512301.1:p.Cys1169Gly
|
|
ENST00000695975.1:c.*1809T>G
|
ENSP00000512302.1:n.*1809T>G
|
|
ENST00000695976.1:c.3493T>G
|
ENSP00000512303.1:p.Cys1165Gly
|
|
ENST00000695981.1:c.3580+102T>G
|
ENSP00000512306.1:n.3580+102T>G
|
|
ENST00000695984.1:c.1690T>G
|
ENSP00000512309.1:p.Cys564Gly
|
|
ENST00000695986.1:c.*3333T>G
|
ENSP00000512311.1:n.*3333T>G
|
|
ENST00000695990.1:n.716T>G
|
|
|
ENST00000696026.1:c.*1964T>G
|
ENSP00000512335.1:n.*1964T>G
|
|
ENST00000696027.1:c.3676T>G
|
ENSP00000512336.1:p.Cys1226Gly
|
|
ENST00000696028.1:c.3610T>G
|
ENSP00000512337.1:p.Cys1204Gly
|
|
ENST00000696029.1:c.3676T>G
|
ENSP00000512338.1:p.Cys1226Gly
|
|
ENST00000696031.1:c.*3200T>G
|
ENSP00000512340.1:n.*3200T>G
|
|
ENST00000696032.1:c.3580+102T>G
|
ENSP00000512341.1:n.3580+102T>G
|
|
ENST00000696033.1:c.1160-32498T>G
|
ENSP00000512342.1:n.1160-32498T>G
|
|
ENST00000367429.9:c.3682T>G
MANE Select
|
ENSP00000356399.4:p.Cys1228Gly
|
|
ENST00000367429.8:c.3682T>G
|
ENSP00000356399.4:p.Cys1228Gly
|
|
ENST00000466229.5:n.6780T>G
|
|
|
NM_000186.3:c.3682T>G , LRG_47t1:c.3682T>G
|
NP_000177.2:p.Cys1228Gly
|
|
XR_001737134.2:n.3868T>G
|
|
|
NM_000186.4:c.3682T>G
MANE Select
|
NP_000177.2:p.Cys1228Gly
|
|