|
ENST00000509514.6:c.593C>G
|
ENSP00000426272.2:p.Ser198Ter
|
|
|
ENST00000518349.6:c.113-17551C>G
|
ENSP00000507185.1:n.113-17551C>G
|
|
|
ENST00000682445.1:c.*474C>G
|
ENSP00000508061.1:n.*474C>G
|
|
|
ENST00000682531.1:n.694C>G
|
|
|
|
ENST00000682626.1:c.*99C>G
|
ENSP00000507857.1:n.*99C>G
|
|
|
ENST00000682996.1:c.593C>G
|
ENSP00000507792.1:p.Ser198Ter
|
|
|
ENST00000683265.1:n.686C>G
|
|
|
|
ENST00000683371.1:c.*723C>G
|
ENSP00000508376.1:n.*723C>G
|
|
|
ENST00000683390.1:n.2283C>G
|
|
|
|
ENST00000683549.1:n.514C>G
|
|
|
|
ENST00000683936.1:c.*478C>G
|
ENSP00000507721.1:n.*478C>G
|
|
|
ENST00000683974.1:n.675C>G
|
|
|
|
ENST00000683996.1:c.182C>G
|
ENSP00000507060.1:p.Ser61Ter
|
|
|
ENST00000684131.1:n.432C>G
|
|
|
|
ENST00000684160.1:c.*283C>G
|
ENSP00000507821.1:n.*283C>G
|
|
|
ENST00000684214.1:c.593C>G
|
ENSP00000508071.1:p.Ser198Ter
|
|
|
ENST00000414835.7:c.668C>G
|
ENSP00000411960.3:p.Ser223Ter
|
|
|
ENST00000510025.7:c.593C>G
MANE Select
|
ENSP00000424940.3:p.Ser198Ter
|
|
|
ENST00000643250.1:c.*465C>G
|
ENSP00000494737.1:n.*465C>G
|
|
|
ENST00000644146.1:c.*171C>G
|
ENSP00000494808.1:n.*171C>G
|
|
|
ENST00000645099.1:c.152C>G
|
ENSP00000496091.1:p.Ser51Ter
|
|
|
ENST00000645702.1:c.182C>G
|
ENSP00000496432.1:p.Ser61Ter
|
|
|
ENST00000645832.1:c.*478C>G
|
ENSP00000494316.1:n.*478C>G
|
|
|
ENST00000646058.1:c.593C>G
|
ENSP00000493579.1:p.Ser198Ter
|
|
|
ENST00000646355.1:c.*599C>G
|
ENSP00000493801.1:n.*599C>G
|
|
|
ENST00000646554.1:c.*571C>G
|
ENSP00000494542.1:n.*571C>G
|
|
|
ENST00000647335.1:c.*560C>G
|
ENSP00000495180.1:n.*560C>G
|
|
|
ENST00000647342.1:c.*524C>G
|
ENSP00000494992.1:n.*524C>G
|
|
|
ENST00000256216.10:c.593C>G
|
ENSP00000256216.6:p.Ser198Ter
|
|
|
ENST00000414835.6:c.173C>G
|
ENSP00000411960.2:p.Ser58Ter
|
|
|
ENST00000442060.7:c.593C>G
|
ENSP00000390208.3:p.Ser198Ter
|
|
|
ENST00000503168.5:n.582C>G
|
|
|
|
ENST00000504811.5:c.668C>G
|
ENSP00000420914.1:p.Ser223Ter
|
|
|
ENST00000505181.5:n.296C>G
|
|
|
|
ENST00000509514.5:c.-292C>G
|
ENSP00000426272.1:n.-292C>G
|
|
|
ENST00000510025.5:c.521C>G
|
ENSP00000424940.1:p.Ser174Ter
|
|
|
ENST00000512644.1:n.161C>G
|
|
|
|
ENST00000513628.5:c.182C>G
|
ENSP00000425993.1:p.Ser61Ter
|
|
|
ENST00000515235.6:n.653C>G
|
|
|
|
ENST00000515320.5:c.539C>G
|
ENSP00000424613.1:p.Ser180Ter
|
|
|
NM_000414.3:c.593C>G
|
NP_000405.1:p.Ser198Ter
|
|
|
NM_001199291.2:c.668C>G
|
NP_001186220.1:p.Ser223Ter
|
|
|
NM_001199292.1:c.539C>G
|
NP_001186221.1:p.Ser180Ter
|
|
|
NM_001292027.1:c.521C>G
|
NP_001278956.1:p.Ser174Ter
|
|
|
NM_001292028.1:c.173C>G
|
NP_001278957.1:p.Ser58Ter
|
|
|
NM_000414.4:c.593C>G
MANE Select
|
NP_000405.1:p.Ser198Ter
|
|
|
NM_001199291.3:c.668C>G
|
NP_001186220.1:p.Ser223Ter
|
|
|
NM_001199292.2:c.539C>G
|
NP_001186221.1:p.Ser180Ter
|
|
|
NM_001292027.2:c.521C>G
|
NP_001278956.1:p.Ser174Ter
|
|
|
NM_001292028.2:c.173C>G
|
NP_001278957.1:p.Ser58Ter
|
|
|
NM_001374497.1:c.584C>G
|
NP_001361426.1:p.Ser195Ter
|
|
|
NM_001374498.1:c.593C>G
|
NP_001361427.1:p.Ser198Ter
|
|
|
NM_001374499.1:c.266C>G
|
NP_001361428.1:p.Ser89Ter
|
|
|
NM_001374500.1:c.152C>G
|
NP_001361429.1:p.Ser51Ter
|
|
|
NM_001374501.1:c.182C>G
|
NP_001361430.1:p.Ser61Ter
|
|
|
NM_001374502.1:c.182C>G
|
NP_001361431.1:p.Ser61Ter
|
|
|
NM_001374503.1:c.182C>G
|
NP_001361432.1:p.Ser61Ter
|
|
|
NR_164653.1:n.672C>G
|
|
|
|
NR_164654.1:n.860C>G
|
|
|
