ENST00000478995.2:n.3232G>C
|
|
|
ENST00000488970.2:n.3871G>C
|
|
|
ENST00000695614.1:c.1715G>C
|
ENSP00000512053.1:p.Ser572Thr
|
|
ENST00000695615.1:c.1715G>C
|
ENSP00000512054.1:p.Ser572Thr
|
|
ENST00000695616.1:c.*1560G>C
|
ENSP00000512055.1:n.*1560G>C
|
|
ENST00000695617.1:c.1712G>C
|
ENSP00000512056.1:p.Ser571Thr
|
|
ENST00000695618.1:c.*1464G>C
|
ENSP00000512058.1:n.*1464G>C
|
|
ENST00000695619.1:c.*1425G>C
|
ENSP00000512059.1:n.*1425G>C
|
|
ENST00000695620.1:c.*1641G>C
|
ENSP00000512060.1:n.*1641G>C
|
|
ENST00000695621.1:c.*140G>C
|
ENSP00000512061.1:n.*140G>C
|
|
ENST00000695622.1:c.1652G>C
|
ENSP00000512062.1:p.Ser551Thr
|
|
ENST00000695623.1:c.1709G>C
|
ENSP00000512063.1:p.Ser570Thr
|
|
ENST00000695624.1:n.1020G>C
|
|
|
ENST00000695625.1:c.1715G>C
|
ENSP00000512064.1:p.Ser572Thr
|
|
ENST00000695626.1:c.470G>C
|
ENSP00000512065.1:n.470G>C
|
|
ENST00000695627.1:c.663G>C
|
ENSP00000512066.1:n.663G>C
|
|
ENST00000695628.1:c.274G>C
|
ENSP00000512067.1:n.274G>C
|
|
ENST00000695629.1:c.191-554G>C
|
ENSP00000512068.1:n.191-554G>C
|
|
ENST00000695630.1:c.442G>C
|
|
|
ENST00000695631.1:c.115-657G>C
|
|
|
ENST00000695632.1:n.515G>C
|
|
|
ENST00000703407.1:c.1187G>C
|
ENSP00000512057.1:p.Ser396Thr
|
|
ENST00000308731.8:c.1715G>C
MANE Select
|
ENSP00000308176.8:p.Ser572Thr
|
|
ENST00000308731.7:c.1715G>C
|
ENSP00000308176.7:p.Ser572Thr
|
|
ENST00000372880.5:c.1187G>C
|
ENSP00000361971.1:p.Ser396Thr
|
|
ENST00000470069.1:n.80G>C
|
|
|
ENST00000488970.1:n.317G>C
|
|
|
ENST00000618050.4:c.1714G>C
|
ENSP00000479125.1:n.1714G>C
|
|
ENST00000621635.4:c.1817G>C
|
ENSP00000483570.1:p.Ser606Thr
|
|
NM_000061.2:c.1715G>C , LRG_128t1:c.1715G>C
|
NP_000052.1:p.Ser572Thr
|
|
NM_001287344.1:c.1817G>C
|
NP_001274273.1:p.Ser606Thr
|
|
NM_001287345.1:c.1187G>C
|
NP_001274274.1:p.Ser396Thr
|
|
NM_000061.3:c.1715G>C
MANE Select
|
NP_000052.1:p.Ser572Thr
|
|
NM_001287344.2:c.1817G>C
|
NP_001274273.1:p.Ser606Thr
|
|
NM_001287345.2:c.1187G>C
|
NP_001274274.1:p.Ser396Thr
|
|