ENST00000478995.2:n.3381G>T
|
|
|
ENST00000488970.2:n.4020G>T
|
|
|
ENST00000695614.1:c.1864G>T
|
ENSP00000512053.1:p.Ala622Ser
|
|
ENST00000695615.1:c.1864G>T
|
ENSP00000512054.1:p.Ala622Ser
|
|
ENST00000695616.1:c.*1709G>T
|
ENSP00000512055.1:n.*1709G>T
|
|
ENST00000695617.1:c.1861G>T
|
ENSP00000512056.1:p.Ala621Ser
|
|
ENST00000695618.1:c.*1613G>T
|
ENSP00000512058.1:n.*1613G>T
|
|
ENST00000695619.1:c.*1574G>T
|
ENSP00000512059.1:n.*1574G>T
|
|
ENST00000695620.1:c.*1790G>T
|
ENSP00000512060.1:n.*1790G>T
|
|
ENST00000695621.1:c.*289G>T
|
ENSP00000512061.1:n.*289G>T
|
|
ENST00000695622.1:c.1801G>T
|
ENSP00000512062.1:p.Ala601Ser
|
|
ENST00000695623.1:c.1858G>T
|
ENSP00000512063.1:p.Ala620Ser
|
|
ENST00000695624.1:n.1169G>T
|
|
|
ENST00000695625.1:c.1864G>T
|
ENSP00000512064.1:p.Ala622Ser
|
|
ENST00000695626.1:c.619G>T
|
ENSP00000512065.1:n.619G>T
|
|
ENST00000695627.1:c.812G>T
|
ENSP00000512066.1:n.812G>T
|
|
ENST00000695628.1:c.423G>T
|
ENSP00000512067.1:n.423G>T
|
|
ENST00000695629.1:c.304G>T
|
ENSP00000512068.1:p.Ala102Ser
|
|
ENST00000695630.1:c.591G>T
|
|
|
ENST00000695631.1:c.125G>T
|
|
|
ENST00000703407.1:c.1336G>T
|
ENSP00000512057.1:p.Ala446Ser
|
|
ENST00000308731.8:c.1864G>T
MANE Select
|
ENSP00000308176.8:p.Ala622Ser
|
|
ENST00000308731.7:c.1864G>T
|
ENSP00000308176.7:p.Ala622Ser
|
|
ENST00000372880.5:c.1336G>T
|
ENSP00000361971.1:p.Ala446Ser
|
|
ENST00000470069.1:n.229G>T
|
|
|
ENST00000618050.4:c.1863G>T
|
ENSP00000479125.1:n.1863G>T
|
|
ENST00000621635.4:c.1966G>T
|
ENSP00000483570.1:p.Ala656Ser
|
|
NM_000061.2:c.1864G>T , LRG_128t1:c.1864G>T
|
NP_000052.1:p.Ala622Ser
|
|
NM_001287344.1:c.1966G>T
|
NP_001274273.1:p.Ala656Ser
|
|
NM_001287345.1:c.1336G>T
|
NP_001274274.1:p.Ala446Ser
|
|
NM_000061.3:c.1864G>T
MANE Select
|
NP_000052.1:p.Ala622Ser
|
|
NM_001287344.2:c.1966G>T
|
NP_001274273.1:p.Ala656Ser
|
|
NM_001287345.2:c.1336G>T
|
NP_001274274.1:p.Ala446Ser
|
|