|
ENST00000478995.2:n.3395A>T
|
|
|
|
ENST00000488970.2:n.4034A>T
|
|
|
|
ENST00000695614.1:c.1878A>T
|
ENSP00000512053.1:p.Val626=
|
|
|
ENST00000695615.1:c.1878A>T
|
ENSP00000512054.1:p.Val626=
|
|
|
ENST00000695616.1:c.*1723A>T
|
ENSP00000512055.1:n.*1723A>T
|
|
|
ENST00000695617.1:c.1875A>T
|
ENSP00000512056.1:p.Val625=
|
|
|
ENST00000695618.1:c.*1627A>T
|
ENSP00000512058.1:n.*1627A>T
|
|
|
ENST00000695619.1:c.*1588A>T
|
ENSP00000512059.1:n.*1588A>T
|
|
|
ENST00000695620.1:c.*1804A>T
|
ENSP00000512060.1:n.*1804A>T
|
|
|
ENST00000695621.1:c.*303A>T
|
ENSP00000512061.1:n.*303A>T
|
|
|
ENST00000695622.1:c.1815A>T
|
ENSP00000512062.1:p.Val605=
|
|
|
ENST00000695623.1:c.1872A>T
|
ENSP00000512063.1:p.Val624=
|
|
|
ENST00000695624.1:n.1183A>T
|
|
|
|
ENST00000695625.1:c.1875+3A>T
|
ENSP00000512064.1:n.1875+3A>T
|
|
|
ENST00000695626.1:c.633A>T
|
ENSP00000512065.1:n.633A>T
|
|
|
ENST00000695627.1:c.826A>T
|
ENSP00000512066.1:n.826A>T
|
|
|
ENST00000695628.1:c.437A>T
|
ENSP00000512067.1:n.437A>T
|
|
|
ENST00000695629.1:c.318A>T
|
ENSP00000512068.1:p.Val106=
|
|
|
ENST00000695630.1:c.605A>T
|
|
|
|
ENST00000695631.1:c.139A>T
|
|
|
|
ENST00000703407.1:c.1350A>T
|
ENSP00000512057.1:p.Val450=
|
|
|
ENST00000308731.8:c.1878A>T
MANE Select
|
ENSP00000308176.8:p.Val626=
|
|
|
ENST00000308731.7:c.1878A>T
|
ENSP00000308176.7:p.Val626=
|
|
|
ENST00000372880.5:c.1350A>T
|
ENSP00000361971.1:p.Val450=
|
|
|
ENST00000470069.1:n.243A>T
|
|
|
|
ENST00000618050.4:c.1877A>T
|
ENSP00000479125.1:n.1877A>T
|
|
|
ENST00000621635.4:c.1980A>T
|
ENSP00000483570.1:p.Val660=
|
|
|
NM_000061.2:c.1878A>T , LRG_128t1:c.1878A>T
|
NP_000052.1:p.Val626=
|
|
|
NM_001287344.1:c.1980A>T
|
NP_001274273.1:p.Val660=
|
|
|
NM_001287345.1:c.1350A>T
|
NP_001274274.1:p.Val450=
|
|
|
NM_000061.3:c.1878A>T
MANE Select
|
NP_000052.1:p.Val626=
|
|
|
NM_001287344.2:c.1980A>T
|
NP_001274273.1:p.Val660=
|
|
|
NM_001287345.2:c.1350A>T
|
NP_001274274.1:p.Val450=
|
|
