|
ENST00000509514.6:c.576T>G
|
ENSP00000426272.2:p.Ile192Met
|
|
|
ENST00000518349.6:c.113-17568T>G
|
ENSP00000507185.1:n.113-17568T>G
|
|
|
ENST00000682445.1:c.*457T>G
|
ENSP00000508061.1:n.*457T>G
|
|
|
ENST00000682531.1:n.677T>G
|
|
|
|
ENST00000682626.1:c.*82T>G
|
ENSP00000507857.1:n.*82T>G
|
|
|
ENST00000682996.1:c.576T>G
|
ENSP00000507792.1:p.Ile192Met
|
|
|
ENST00000683265.1:n.669T>G
|
|
|
|
ENST00000683371.1:c.*706T>G
|
ENSP00000508376.1:n.*706T>G
|
|
|
ENST00000683390.1:n.2266T>G
|
|
|
|
ENST00000683549.1:n.497T>G
|
|
|
|
ENST00000683936.1:c.*461T>G
|
ENSP00000507721.1:n.*461T>G
|
|
|
ENST00000683974.1:n.658T>G
|
|
|
|
ENST00000683996.1:c.165T>G
|
ENSP00000507060.1:p.Ile55Met
|
|
|
ENST00000684131.1:n.415T>G
|
|
|
|
ENST00000684160.1:c.*266T>G
|
ENSP00000507821.1:n.*266T>G
|
|
|
ENST00000684214.1:c.576T>G
|
ENSP00000508071.1:p.Ile192Met
|
|
|
ENST00000414835.7:c.651T>G
|
ENSP00000411960.3:p.Ile217Met
|
|
|
ENST00000510025.7:c.576T>G
MANE Select
|
ENSP00000424940.3:p.Ile192Met
|
|
|
ENST00000643250.1:c.*448T>G
|
ENSP00000494737.1:n.*448T>G
|
|
|
ENST00000644146.1:c.*154T>G
|
ENSP00000494808.1:n.*154T>G
|
|
|
ENST00000645099.1:c.135T>G
|
ENSP00000496091.1:p.Ile45Met
|
|
|
ENST00000645702.1:c.165T>G
|
ENSP00000496432.1:p.Ile55Met
|
|
|
ENST00000645832.1:c.*461T>G
|
ENSP00000494316.1:n.*461T>G
|
|
|
ENST00000646058.1:c.576T>G
|
ENSP00000493579.1:p.Ile192Met
|
|
|
ENST00000646355.1:c.*582T>G
|
ENSP00000493801.1:n.*582T>G
|
|
|
ENST00000646554.1:c.*554T>G
|
ENSP00000494542.1:n.*554T>G
|
|
|
ENST00000647335.1:c.*543T>G
|
ENSP00000495180.1:n.*543T>G
|
|
|
ENST00000647342.1:c.*507T>G
|
ENSP00000494992.1:n.*507T>G
|
|
|
ENST00000256216.10:c.576T>G
|
ENSP00000256216.6:p.Ile192Met
|
|
|
ENST00000414835.6:c.156T>G
|
ENSP00000411960.2:p.Ile52Met
|
|
|
ENST00000442060.7:c.576T>G
|
ENSP00000390208.3:p.Ile192Met
|
|
|
ENST00000503168.5:n.565T>G
|
|
|
|
ENST00000504811.5:c.651T>G
|
ENSP00000420914.1:p.Ile217Met
|
|
|
ENST00000505181.5:n.279T>G
|
|
|
|
ENST00000509514.5:c.-309T>G
|
ENSP00000426272.1:n.-309T>G
|
|
|
ENST00000510025.5:c.504T>G
|
ENSP00000424940.1:p.Ile168Met
|
|
|
ENST00000512644.1:n.144T>G
|
|
|
|
ENST00000513628.5:c.165T>G
|
ENSP00000425993.1:p.Ile55Met
|
|
|
ENST00000515235.6:n.636T>G
|
|
|
|
ENST00000515320.5:c.522T>G
|
ENSP00000424613.1:p.Ile174Met
|
|
|
NM_000414.3:c.576T>G
|
NP_000405.1:p.Ile192Met
|
|
|
NM_001199291.2:c.651T>G
|
NP_001186220.1:p.Ile217Met
|
|
|
NM_001199292.1:c.522T>G
|
NP_001186221.1:p.Ile174Met
|
|
|
NM_001292027.1:c.504T>G
|
NP_001278956.1:p.Ile168Met
|
|
|
NM_001292028.1:c.156T>G
|
NP_001278957.1:p.Ile52Met
|
|
|
NM_000414.4:c.576T>G
MANE Select
|
NP_000405.1:p.Ile192Met
|
|
|
NM_001199291.3:c.651T>G
|
NP_001186220.1:p.Ile217Met
|
|
|
NM_001199292.2:c.522T>G
|
NP_001186221.1:p.Ile174Met
|
|
|
NM_001292027.2:c.504T>G
|
NP_001278956.1:p.Ile168Met
|
|
|
NM_001292028.2:c.156T>G
|
NP_001278957.1:p.Ile52Met
|
|
|
NM_001374497.1:c.567T>G
|
NP_001361426.1:p.Ile189Met
|
|
|
NM_001374498.1:c.576T>G
|
NP_001361427.1:p.Ile192Met
|
|
|
NM_001374499.1:c.249T>G
|
NP_001361428.1:p.Ile83Met
|
|
|
NM_001374500.1:c.135T>G
|
NP_001361429.1:p.Ile45Met
|
|
|
NM_001374501.1:c.165T>G
|
NP_001361430.1:p.Ile55Met
|
|
|
NM_001374502.1:c.165T>G
|
NP_001361431.1:p.Ile55Met
|
|
|
NM_001374503.1:c.165T>G
|
NP_001361432.1:p.Ile55Met
|
|
|
NR_164653.1:n.655T>G
|
|
|
|
NR_164654.1:n.843T>G
|
|
|
