ENST00000278379.9:c.1686C>T
MANE Select
|
ENSP00000278379.3:p.Asp562=
|
|
ENST00000395750.6:c.1674C>T
|
ENSP00000379099.2:p.Asp558=
|
|
ENST00000395753.6:c.1659C>T
|
ENSP00000379102.1:p.Asp553=
|
|
ENST00000479543.2:n.1238C>T
|
|
|
ENST00000642171.1:c.*68C>T
|
ENSP00000495538.1:n.*68C>T
|
|
ENST00000642448.1:n.1778C>T
|
|
|
ENST00000642769.1:c.952C>T
|
|
|
ENST00000643000.1:c.1659C>T
|
ENSP00000495164.1:p.Asp553=
|
|
ENST00000643134.1:c.1673C>T
|
ENSP00000495188.1:p.Thr558Ile
|
|
ENST00000643522.1:c.1452C>T
|
ENSP00000496375.1:p.Asp484=
|
|
ENST00000644050.1:c.1659C>T
|
ENSP00000496123.1:p.Asp553=
|
|
ENST00000644299.1:c.1659C>T
|
ENSP00000494669.1:p.Asp553=
|
|
ENST00000644459.1:c.*178C>T
|
ENSP00000495861.1:n.*178C>T
|
|
ENST00000644779.1:c.1797C>T
|
ENSP00000494258.1:p.Asp599=
|
|
ENST00000644868.1:c.1748C>T
|
ENSP00000496760.1:n.1748C>T
|
|
ENST00000645194.1:c.1659C>T
|
ENSP00000496093.1:p.Asp553=
|
|
ENST00000645303.1:c.1701C>T
|
ENSP00000496667.1:p.Asp567=
|
|
ENST00000645542.1:n.392C>T
|
|
|
ENST00000645634.1:c.1659C>T
|
ENSP00000493945.1:p.Asp553=
|
|
ENST00000646080.1:c.1677C>T
|
ENSP00000494113.1:p.Asp559=
|
|
ENST00000647076.1:c.427C>T
|
|
|
ENST00000647104.1:c.1659C>T
|
ENSP00000494025.1:p.Asp553=
|
|
ENST00000278379.7:c.1686C>T
|
ENSP00000278379.3:p.Asp562=
|
|
ENST00000395750.5:c.1659C>T
|
ENSP00000379099.1:p.Asp553=
|
|
ENST00000395753.5:c.1659C>T
|
ENSP00000379102.1:p.Asp553=
|
|
ENST00000464522.2:c.219+4594C>T
|
ENSP00000435406.1:n.219+4594C>T
|
|
ENST00000479543.1:n.502C>T
|
|
|
NM_001195728.2:c.1659C>T
|
NP_001182657.1:p.Asp553=
|
|
NM_001252652.1:c.1659C>T
|
NP_001239581.1:p.Asp553=
|
|
NM_004171.3:c.1686C>T
|
NP_004162.2:p.Asp562=
|
|
XM_005253067.1:c.1677C>T
|
XP_005253124.1:p.Asp559=
|
|
XM_011520284.1:c.1734C>T
|
XP_011518586.1:p.Asp578=
|
|
XM_011520285.1:c.1674C>T
|
XP_011518587.1:p.Asp558=
|
|
XM_011520286.1:c.1599C>T
|
XP_011518588.1:p.Asp533=
|
|
XM_011520287.1:c.1500C>T
|
XP_011518589.1:p.Asp500=
|
|
XM_011520285.2:c.1674C>T
|
XP_011518587.1:p.Asp558=
|
|
XM_017018136.1:c.1701C>T
|
XP_016873625.1:p.Asp567=
|
|
XM_017018137.1:c.1659C>T
|
XP_016873626.1:p.Asp553=
|
|
XM_017018138.1:c.1659C>T
|
XP_016873627.1:p.Asp553=
|
|
XM_017018139.1:c.1452C>T
|
XP_016873628.1:p.Asp484=
|
|
NM_004171.4:c.1686C>T
MANE Select
|
NP_004162.2:p.Asp562=
|
|
NM_001195728.3:c.1659C>T
|
NP_001182657.1:p.Asp553=
|
|
NM_001252652.2:c.1659C>T
|
NP_001239581.1:p.Asp553=
|
|