ENST00000470918.2:n.4522A>G
|
|
|
ENST00000695970.1:c.3320A>G
|
ENSP00000512297.1:p.His1107Arg
|
|
ENST00000695971.1:c.3473A>G
|
ENSP00000512298.1:p.His1158Arg
|
|
ENST00000695972.1:c.*571A>G
|
ENSP00000512299.1:n.*571A>G
|
|
ENST00000695973.1:c.*1858A>G
|
ENSP00000512300.1:n.*1858A>G
|
|
ENST00000695974.1:c.3317A>G
|
ENSP00000512301.1:p.His1106Arg
|
|
ENST00000695975.1:c.*1621A>G
|
ENSP00000512302.1:n.*1621A>G
|
|
ENST00000695976.1:c.3305A>G
|
ENSP00000512303.1:p.His1102Arg
|
|
ENST00000695981.1:c.3494A>G
|
ENSP00000512306.1:p.His1165Arg
|
|
ENST00000695984.1:c.1502A>G
|
ENSP00000512309.1:p.His501Arg
|
|
ENST00000695986.1:c.*3145A>G
|
ENSP00000512311.1:n.*3145A>G
|
|
ENST00000695990.1:n.528A>G
|
|
|
ENST00000696026.1:c.*1776A>G
|
ENSP00000512335.1:n.*1776A>G
|
|
ENST00000696027.1:c.3488A>G
|
ENSP00000512336.1:p.His1163Arg
|
|
ENST00000696028.1:c.3422A>G
|
ENSP00000512337.1:p.His1141Arg
|
|
ENST00000696029.1:c.3488A>G
|
ENSP00000512338.1:p.His1163Arg
|
|
ENST00000696031.1:c.*3012A>G
|
ENSP00000512340.1:n.*3012A>G
|
|
ENST00000696032.1:c.3494A>G
|
ENSP00000512341.1:p.His1165Arg
|
|
ENST00000696033.1:c.1160-32686A>G
|
ENSP00000512342.1:n.1160-32686A>G
|
|
ENST00000367429.9:c.3494A>G
MANE Select
|
ENSP00000356399.4:p.His1165Arg
|
|
ENST00000367429.8:c.3494A>G
|
ENSP00000356399.4:p.His1165Arg
|
|
ENST00000466229.5:n.6592A>G
|
|
|
NM_000186.3:c.3494A>G , LRG_47t1:c.3494A>G
|
NP_000177.2:p.His1165Arg
|
|
XR_001737134.2:n.3680A>G
|
|
|
NM_000186.4:c.3494A>G
MANE Select
|
NP_000177.2:p.His1165Arg
|
|