ENST00000509514.6:c.554G>C
|
ENSP00000426272.2:p.Ser185Thr
|
|
ENST00000518349.6:c.113-17590G>C
|
ENSP00000507185.1:n.113-17590G>C
|
|
ENST00000682445.1:c.*435G>C
|
ENSP00000508061.1:n.*435G>C
|
|
ENST00000682531.1:n.655G>C
|
|
|
ENST00000682626.1:c.*60G>C
|
ENSP00000507857.1:n.*60G>C
|
|
ENST00000682996.1:c.554G>C
|
ENSP00000507792.1:p.Ser185Thr
|
|
ENST00000683265.1:n.647G>C
|
|
|
ENST00000683371.1:c.*684G>C
|
ENSP00000508376.1:n.*684G>C
|
|
ENST00000683390.1:n.2244G>C
|
|
|
ENST00000683549.1:n.475G>C
|
|
|
ENST00000683936.1:c.*439G>C
|
ENSP00000507721.1:n.*439G>C
|
|
ENST00000683974.1:n.636G>C
|
|
|
ENST00000683996.1:c.143G>C
|
ENSP00000507060.1:p.Ser48Thr
|
|
ENST00000684131.1:n.393G>C
|
|
|
ENST00000684160.1:c.*244G>C
|
ENSP00000507821.1:n.*244G>C
|
|
ENST00000684214.1:c.554G>C
|
ENSP00000508071.1:p.Ser185Thr
|
|
ENST00000414835.7:c.629G>C
|
ENSP00000411960.3:p.Ser210Thr
|
|
ENST00000510025.7:c.554G>C
MANE Select
|
ENSP00000424940.3:p.Ser185Thr
|
|
ENST00000643250.1:c.*426G>C
|
ENSP00000494737.1:n.*426G>C
|
|
ENST00000644146.1:c.*132G>C
|
ENSP00000494808.1:n.*132G>C
|
|
ENST00000645099.1:c.113G>C
|
ENSP00000496091.1:p.Ser38Thr
|
|
ENST00000645702.1:c.143G>C
|
ENSP00000496432.1:p.Ser48Thr
|
|
ENST00000645832.1:c.*439G>C
|
ENSP00000494316.1:n.*439G>C
|
|
ENST00000646058.1:c.554G>C
|
ENSP00000493579.1:p.Ser185Thr
|
|
ENST00000646355.1:c.*560G>C
|
ENSP00000493801.1:n.*560G>C
|
|
ENST00000646554.1:c.*532G>C
|
ENSP00000494542.1:n.*532G>C
|
|
ENST00000647335.1:c.*521G>C
|
ENSP00000495180.1:n.*521G>C
|
|
ENST00000647342.1:c.*485G>C
|
ENSP00000494992.1:n.*485G>C
|
|
ENST00000256216.10:c.554G>C
|
ENSP00000256216.6:p.Ser185Thr
|
|
ENST00000414835.6:c.134G>C
|
ENSP00000411960.2:p.Ser45Thr
|
|
ENST00000442060.7:c.554G>C
|
ENSP00000390208.3:p.Ser185Thr
|
|
ENST00000503168.5:n.543G>C
|
|
|
ENST00000504811.5:c.629G>C
|
ENSP00000420914.1:p.Ser210Thr
|
|
ENST00000505181.5:n.257G>C
|
|
|
ENST00000509514.5:c.-331G>C
|
ENSP00000426272.1:n.-331G>C
|
|
ENST00000510025.5:c.482G>C
|
ENSP00000424940.1:p.Ser161Thr
|
|
ENST00000512644.1:n.122G>C
|
|
|
ENST00000513628.5:c.143G>C
|
ENSP00000425993.1:p.Ser48Thr
|
|
ENST00000515235.6:n.614G>C
|
|
|
ENST00000515320.5:c.500G>C
|
ENSP00000424613.1:p.Ser167Thr
|
|
NM_000414.3:c.554G>C
|
NP_000405.1:p.Ser185Thr
|
|
NM_001199291.2:c.629G>C
|
NP_001186220.1:p.Ser210Thr
|
|
NM_001199292.1:c.500G>C
|
NP_001186221.1:p.Ser167Thr
|
|
NM_001292027.1:c.482G>C
|
NP_001278956.1:p.Ser161Thr
|
|
NM_001292028.1:c.134G>C
|
NP_001278957.1:p.Ser45Thr
|
|
NM_000414.4:c.554G>C
MANE Select
|
NP_000405.1:p.Ser185Thr
|
|
NM_001199291.3:c.629G>C
|
NP_001186220.1:p.Ser210Thr
|
|
NM_001199292.2:c.500G>C
|
NP_001186221.1:p.Ser167Thr
|
|
NM_001292027.2:c.482G>C
|
NP_001278956.1:p.Ser161Thr
|
|
NM_001292028.2:c.134G>C
|
NP_001278957.1:p.Ser45Thr
|
|
NM_001374497.1:c.545G>C
|
NP_001361426.1:p.Ser182Thr
|
|
NM_001374498.1:c.554G>C
|
NP_001361427.1:p.Ser185Thr
|
|
NM_001374499.1:c.227G>C
|
NP_001361428.1:p.Ser76Thr
|
|
NM_001374500.1:c.113G>C
|
NP_001361429.1:p.Ser38Thr
|
|
NM_001374501.1:c.143G>C
|
NP_001361430.1:p.Ser48Thr
|
|
NM_001374502.1:c.143G>C
|
NP_001361431.1:p.Ser48Thr
|
|
NM_001374503.1:c.143G>C
|
NP_001361432.1:p.Ser48Thr
|
|
NR_164653.1:n.633G>C
|
|
|
NR_164654.1:n.821G>C
|
|
|