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ENST00000697148.1:c.1009G=
|
ENSP00000513137.1:n.1009G=
|
|
|
ENST00000697149.1:c.972G=
|
ENSP00000513138.1:n.972G=
|
|
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ENST00000697150.1:c.1045+3464G=
|
ENSP00000513139.1:n.1045+3464G=
|
|
|
ENST00000697151.1:c.1045+3464G=
|
ENSP00000513140.1:n.1045+3464G=
|
|
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ENST00000697152.1:c.799-15571G=
|
ENSP00000513141.1:n.799-15571G=
|
|
|
ENST00000697153.1:c.795-15571G=
|
ENSP00000513142.1:n.795-15571G=
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|
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ENST00000697154.1:c.956-18212G=
|
ENSP00000513143.1:n.956-18212G=
|
|
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ENST00000697155.1:c.649-18212G=
|
ENSP00000513144.1:n.649-18212G=
|
|
|
ENST00000697156.1:c.1133G=
|
ENSP00000513145.1:p.Arg378=
|
|
|
ENST00000697157.1:c.987G=
|
ENSP00000513146.1:n.987G=
|
|
|
ENST00000697158.1:c.976G=
|
ENSP00000513147.1:n.976G=
|
|
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ENST00000697159.1:c.826G=
|
ENSP00000513148.1:n.826G=
|
|
|
ENST00000697160.1:c.956-15571G=
|
ENSP00000513149.1:n.956-15571G=
|
|
|
ENST00000697161.1:c.669G=
|
ENSP00000513150.1:n.669G=
|
|
|
ENST00000697162.1:c.1062G=
|
ENSP00000513151.1:n.1062G=
|
|
|
ENST00000697163.1:c.1133G=
|
ENSP00000513152.1:p.Arg378=
|
|
|
ENST00000697164.1:c.1043G=
|
ENSP00000513153.1:p.Arg348=
|
|
|
ENST00000697165.1:c.830G=
|
ENSP00000513154.1:p.Arg277=
|
|
|
ENST00000697223.1:c.882G=
|
ENSP00000513190.1:n.882G=
|
|
|
ENST00000697224.1:c.884+3464G=
|
ENSP00000513191.1:n.884+3464G=
|
|
|
ENST00000697225.1:c.736G=
|
ENSP00000513192.1:n.736G=
|
|
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ENST00000697226.1:c.738+3464G=
|
ENSP00000513193.1:n.738+3464G=
|
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|
ENST00000697227.1:c.969G=
|
ENSP00000513194.1:n.969G=
|
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ENST00000697228.1:c.825G=
|
ENSP00000513195.1:n.825G=
|
|
|
ENST00000697229.1:c.885-15571G=
|
ENSP00000513196.1:n.885-15571G=
|
|
|
ENST00000697230.1:c.1043G=
|
ENSP00000513197.1:p.Arg348=
|
|
|
ENST00000697231.1:c.1038G=
|
ENSP00000513198.1:n.1038G=
|
|
|
ENST00000697232.1:c.1062G=
|
ENSP00000513199.1:n.1062G=
|
|
|
ENST00000347310.10:c.1133G=
MANE Select
|
ENSP00000321345.5:p.Arg378=
|
|
|
ENST00000637002.1:c.524G=
|
ENSP00000490340.1:p.Arg175=
|
|
|
ENST00000347310.9:c.1133G=
|
ENSP00000321345.5:p.Arg378=
|
|
|
ENST00000395227.2:c.-58-15571G=
|
ENSP00000378652.2:n.-58-15571G=
|
|
|
ENST00000425614.3:c.368G=
|
ENSP00000387640.2:p.Arg123=
|
|
|
ENST00000473881.2:c.191-15571G=
|
ENSP00000486667.1:n.191-15571G=
|
|
|
NM_144701.2:c.1133G=
|
NP_653302.2:p.Arg378=
|
|
|
XM_005270516.2:c.371G=
|
XP_005270573.1:p.Arg124=
|
|
|
XM_011540789.1:c.1223G=
|
XP_011539091.1:p.Arg408=
|
|
|
XM_011540790.1:c.1133G=
|
XP_011539092.1:p.Arg378=
|
|
|
XM_011540791.1:c.1133G=
|
XP_011539093.1:p.Arg378=
|
|
|
XM_011540790.3:c.1133G=
|
XP_011539092.1:p.Arg378=
|
|
|
XM_011540791.3:c.1133G=
|
XP_011539093.1:p.Arg378=
|
|
|
XR_001736993.1:n.1228+3464G=
|
|
|
|
NM_144701.3:c.1133G=
MANE Select
|
NP_653302.2:p.Arg378=
|
|
