|
ENST00000509514.6:c.454G=
|
ENSP00000426272.2:p.Ala152=
|
|
|
ENST00000518349.6:c.113-17690G=
|
ENSP00000507185.1:n.113-17690G=
|
|
|
ENST00000682445.1:c.*335G=
|
ENSP00000508061.1:n.*335G=
|
|
|
ENST00000682531.1:n.555G=
|
|
|
|
ENST00000682626.1:c.482G=
|
ENSP00000507857.1:p.Ser161=
|
|
|
ENST00000682996.1:c.454G=
|
ENSP00000507792.1:p.Ala152=
|
|
|
ENST00000683265.1:n.547G=
|
|
|
|
ENST00000683371.1:c.*584G=
|
ENSP00000508376.1:n.*584G=
|
|
|
ENST00000683390.1:n.2144G=
|
|
|
|
ENST00000683549.1:n.375G=
|
|
|
|
ENST00000683936.1:c.*339G=
|
ENSP00000507721.1:n.*339G=
|
|
|
ENST00000683974.1:n.536G=
|
|
|
|
ENST00000683996.1:c.43G=
|
ENSP00000507060.1:p.Ala15=
|
|
|
ENST00000684131.1:n.293G=
|
|
|
|
ENST00000684160.1:c.*144G=
|
ENSP00000507821.1:n.*144G=
|
|
|
ENST00000684214.1:c.454G=
|
ENSP00000508071.1:p.Ala152=
|
|
|
ENST00000414835.7:c.529G=
|
ENSP00000411960.3:p.Ala177=
|
|
|
ENST00000510025.7:c.454G=
MANE Select
|
ENSP00000424940.3:p.Ala152=
|
|
|
ENST00000643250.1:c.*326G=
|
ENSP00000494737.1:n.*326G=
|
|
|
ENST00000644146.1:c.*32G=
|
ENSP00000494808.1:n.*32G=
|
|
|
ENST00000645099.1:c.13G=
|
ENSP00000496091.1:p.Ala5=
|
|
|
ENST00000645702.1:c.43G=
|
ENSP00000496432.1:p.Ala15=
|
|
|
ENST00000645832.1:c.*339G=
|
ENSP00000494316.1:n.*339G=
|
|
|
ENST00000646058.1:c.454G=
|
ENSP00000493579.1:p.Ala152=
|
|
|
ENST00000646355.1:c.*460G=
|
ENSP00000493801.1:n.*460G=
|
|
|
ENST00000646554.1:c.*432G=
|
ENSP00000494542.1:n.*432G=
|
|
|
ENST00000646590.1:c.445G=
|
ENSP00000494892.1:p.Ala149=
|
|
|
ENST00000647335.1:c.*421G=
|
ENSP00000495180.1:n.*421G=
|
|
|
ENST00000647342.1:c.*385G=
|
ENSP00000494992.1:n.*385G=
|
|
|
ENST00000256216.10:c.454G=
|
ENSP00000256216.6:p.Ala152=
|
|
|
ENST00000414835.6:c.34G=
|
ENSP00000411960.2:p.Ala12=
|
|
|
ENST00000442060.7:c.454G=
|
ENSP00000390208.3:p.Ala152=
|
|
|
ENST00000503168.5:n.443G=
|
|
|
|
ENST00000504811.5:c.529G=
|
ENSP00000420914.1:p.Ala177=
|
|
|
ENST00000505181.5:n.157G=
|
|
|
|
ENST00000508788.5:n.356G=
|
|
|
|
ENST00000509514.5:c.-431G=
|
ENSP00000426272.1:n.-431G=
|
|
|
ENST00000510025.5:c.382G=
|
ENSP00000424940.1:p.Ala128=
|
|
|
ENST00000512644.1:n.22G=
|
|
|
|
ENST00000512841.5:n.502G=
|
|
|
|
ENST00000513628.5:c.43G=
|
ENSP00000425993.1:p.Ala15=
|
|
|
ENST00000515235.6:n.514G=
|
|
|
|
ENST00000515320.5:c.400G=
|
ENSP00000424613.1:p.Ala134=
|
|
|
NM_000414.3:c.454G=
|
NP_000405.1:p.Ala152=
|
|
|
NM_001199291.2:c.529G=
|
NP_001186220.1:p.Ala177=
|
|
|
NM_001199292.1:c.400G=
|
NP_001186221.1:p.Ala134=
|
|
|
NM_001292027.1:c.382G=
|
NP_001278956.1:p.Ala128=
|
|
|
NM_001292028.1:c.34G=
|
NP_001278957.1:p.Ala12=
|
|
|
NM_000414.4:c.454G=
MANE Select
|
NP_000405.1:p.Ala152=
|
|
|
NM_001199291.3:c.529G=
|
NP_001186220.1:p.Ala177=
|
|
|
NM_001199292.2:c.400G=
|
NP_001186221.1:p.Ala134=
|
|
|
NM_001292027.2:c.382G=
|
NP_001278956.1:p.Ala128=
|
|
|
NM_001292028.2:c.34G=
|
NP_001278957.1:p.Ala12=
|
|
|
NM_001374497.1:c.445G=
|
NP_001361426.1:p.Ala149=
|
|
|
NM_001374498.1:c.454G=
|
NP_001361427.1:p.Ala152=
|
|
|
NM_001374499.1:c.127G=
|
NP_001361428.1:p.Ala43=
|
|
|
NM_001374500.1:c.13G=
|
NP_001361429.1:p.Ala5=
|
|
|
NM_001374501.1:c.43G=
|
NP_001361430.1:p.Ala15=
|
|
|
NM_001374502.1:c.43G=
|
NP_001361431.1:p.Ala15=
|
|
|
NM_001374503.1:c.43G=
|
NP_001361432.1:p.Ala15=
|
|
|
NR_164653.1:n.533G=
|
|
|
|
NR_164654.1:n.721G=
|
|
|
