|
ENST00000478995.2:n.3236G=
|
|
|
|
ENST00000488970.2:n.3875G=
|
|
|
|
ENST00000695614.1:c.1719G=
|
ENSP00000512053.1:p.Lys573=
|
|
|
ENST00000695615.1:c.1719G=
|
ENSP00000512054.1:p.Lys573=
|
|
|
ENST00000695616.1:c.*1564G=
|
ENSP00000512055.1:n.*1564G=
|
|
|
ENST00000695617.1:c.1716G=
|
ENSP00000512056.1:p.Lys572=
|
|
|
ENST00000695618.1:c.*1468G=
|
ENSP00000512058.1:n.*1468G=
|
|
|
ENST00000695619.1:c.*1429G=
|
ENSP00000512059.1:n.*1429G=
|
|
|
ENST00000695620.1:c.*1645G=
|
ENSP00000512060.1:n.*1645G=
|
|
|
ENST00000695621.1:c.*144G=
|
ENSP00000512061.1:n.*144G=
|
|
|
ENST00000695622.1:c.1656G=
|
ENSP00000512062.1:p.Lys552=
|
|
|
ENST00000695623.1:c.1713G=
|
ENSP00000512063.1:p.Lys571=
|
|
|
ENST00000695624.1:n.1024G=
|
|
|
|
ENST00000695625.1:c.1719G=
|
ENSP00000512064.1:p.Lys573=
|
|
|
ENST00000695626.1:c.474G=
|
ENSP00000512065.1:n.474G=
|
|
|
ENST00000695627.1:c.667G=
|
ENSP00000512066.1:n.667G=
|
|
|
ENST00000695628.1:c.278G=
|
ENSP00000512067.1:n.278G=
|
|
|
ENST00000695629.1:c.191-550G=
|
ENSP00000512068.1:n.191-550G=
|
|
|
ENST00000695630.1:c.446G=
|
|
|
|
ENST00000695631.1:c.115-653G=
|
|
|
|
ENST00000695632.1:n.519G=
|
|
|
|
ENST00000703407.1:c.1191G=
|
ENSP00000512057.1:p.Lys397=
|
|
|
ENST00000308731.8:c.1719G=
MANE Select
|
ENSP00000308176.8:p.Lys573=
|
|
|
ENST00000308731.7:c.1719G=
|
ENSP00000308176.7:p.Lys573=
|
|
|
ENST00000372880.5:c.1191G=
|
ENSP00000361971.1:p.Lys397=
|
|
|
ENST00000470069.1:n.84G=
|
|
|
|
ENST00000488970.1:n.321G=
|
|
|
|
ENST00000618050.4:c.1718G=
|
ENSP00000479125.1:n.1718G=
|
|
|
ENST00000621635.4:c.1821G=
|
ENSP00000483570.1:p.Lys607=
|
|
|
NM_000061.2:c.1719G= , LRG_128t1:c.1719G=
|
NP_000052.1:p.Lys573=
|
|
|
NM_001287344.1:c.1821G=
|
NP_001274273.1:p.Lys607=
|
|
|
NM_001287345.1:c.1191G=
|
NP_001274274.1:p.Lys397=
|
|
|
NM_000061.3:c.1719G=
MANE Select
|
NP_000052.1:p.Lys573=
|
|
|
NM_001287344.2:c.1821G=
|
NP_001274273.1:p.Lys607=
|
|
|
NM_001287345.2:c.1191G=
|
NP_001274274.1:p.Lys397=
|
|
