ENST00000278379.9:c.1723T>G
MANE Select
|
ENSP00000278379.3:p.Ter575Glu
|
|
ENST00000395750.6:c.1711T>G
|
ENSP00000379099.2:p.Ter571Glu
|
|
ENST00000395753.6:c.1696T>G
|
ENSP00000379102.1:p.Ter566Glu
|
|
ENST00000479543.2:n.1275T>G
|
|
|
ENST00000642171.1:c.*105T>G
|
ENSP00000495538.1:n.*105T>G
|
|
ENST00000642448.1:n.1815T>G
|
|
|
ENST00000642769.1:c.989T>G
|
|
|
ENST00000643000.1:c.1696T>G
|
ENSP00000495164.1:p.Ter566Glu
|
|
ENST00000643134.1:c.1710T>G
|
ENSP00000495188.1:p.Asn570Lys
|
|
ENST00000643522.1:c.1489T>G
|
ENSP00000496375.1:p.Ter497Glu
|
|
ENST00000644050.1:c.1696T>G
|
ENSP00000496123.1:p.Ter566Glu
|
|
ENST00000644299.1:c.1696T>G
|
ENSP00000494669.1:p.Ter566Glu
|
|
ENST00000644459.1:c.*215T>G
|
ENSP00000495861.1:n.*215T>G
|
|
ENST00000644779.1:c.1834T>G
|
ENSP00000494258.1:p.Ter612Glu
|
|
ENST00000644868.1:c.1785T>G
|
ENSP00000496760.1:n.1785T>G
|
|
ENST00000645194.1:c.1696T>G
|
ENSP00000496093.1:p.Ter566Glu
|
|
ENST00000645303.1:c.1738T>G
|
ENSP00000496667.1:p.Ter580Glu
|
|
ENST00000645542.1:n.429T>G
|
|
|
ENST00000645634.1:c.1696T>G
|
ENSP00000493945.1:p.Ter566Glu
|
|
ENST00000646080.1:c.1714T>G
|
ENSP00000494113.1:p.Ter572Glu
|
|
ENST00000647076.1:c.464T>G
|
|
|
ENST00000647104.1:c.1696T>G
|
ENSP00000494025.1:p.Ter566Glu
|
|
ENST00000278379.7:c.1723T>G
|
ENSP00000278379.3:p.Ter575Glu
|
|
ENST00000395750.5:c.1696T>G
|
ENSP00000379099.1:p.Ter566Glu
|
|
ENST00000395753.5:c.1696T>G
|
ENSP00000379102.1:p.Ter566Glu
|
|
ENST00000464522.2:c.219+4631T>G
|
ENSP00000435406.1:n.219+4631T>G
|
|
ENST00000479543.1:n.539T>G
|
|
|
NM_001195728.2:c.1696T>G
|
NP_001182657.1:p.Ter566Glu
|
|
NM_001252652.1:c.1696T>G
|
NP_001239581.1:p.Ter566Glu
|
|
NM_004171.3:c.1723T>G
|
NP_004162.2:p.Ter575Glu
|
|
XM_005253067.1:c.1714T>G
|
XP_005253124.1:p.Ter572Glu
|
|
XM_011520284.1:c.1771T>G
|
XP_011518586.1:p.Ter591Glu
|
|
XM_011520285.1:c.1711T>G
|
XP_011518587.1:p.Ter571Glu
|
|
XM_011520286.1:c.1636T>G
|
XP_011518588.1:p.Ter546Glu
|
|
XM_011520287.1:c.1537T>G
|
XP_011518589.1:p.Ter513Glu
|
|
XM_011520285.2:c.1711T>G
|
XP_011518587.1:p.Ter571Glu
|
|
XM_017018136.1:c.1738T>G
|
XP_016873625.1:p.Ter580Glu
|
|
XM_017018137.1:c.1696T>G
|
XP_016873626.1:p.Ter566Glu
|
|
XM_017018138.1:c.1696T>G
|
XP_016873627.1:p.Ter566Glu
|
|
XM_017018139.1:c.1489T>G
|
XP_016873628.1:p.Ter497Glu
|
|
NM_004171.4:c.1723T>G
MANE Select
|
NP_004162.2:p.Ter575Glu
|
|
NM_001195728.3:c.1696T>G
|
NP_001182657.1:p.Ter566Glu
|
|
NM_001252652.2:c.1696T>G
|
NP_001239581.1:p.Ter566Glu
|
|