ENST00000478995.2:n.3282G>C
|
|
|
ENST00000488970.2:n.3921G>C
|
|
|
ENST00000695614.1:c.1765G>C
|
ENSP00000512053.1:p.Glu589Gln
|
|
ENST00000695615.1:c.1765G>C
|
ENSP00000512054.1:p.Glu589Gln
|
|
ENST00000695616.1:c.*1610G>C
|
ENSP00000512055.1:n.*1610G>C
|
|
ENST00000695617.1:c.1762G>C
|
ENSP00000512056.1:p.Glu588Gln
|
|
ENST00000695618.1:c.*1514G>C
|
ENSP00000512058.1:n.*1514G>C
|
|
ENST00000695619.1:c.*1475G>C
|
ENSP00000512059.1:n.*1475G>C
|
|
ENST00000695620.1:c.*1691G>C
|
ENSP00000512060.1:n.*1691G>C
|
|
ENST00000695621.1:c.*190G>C
|
ENSP00000512061.1:n.*190G>C
|
|
ENST00000695622.1:c.1702G>C
|
ENSP00000512062.1:p.Glu568Gln
|
|
ENST00000695623.1:c.1759G>C
|
ENSP00000512063.1:p.Glu587Gln
|
|
ENST00000695624.1:n.1070G>C
|
|
|
ENST00000695625.1:c.1765G>C
|
ENSP00000512064.1:p.Glu589Gln
|
|
ENST00000695626.1:c.520G>C
|
ENSP00000512065.1:n.520G>C
|
|
ENST00000695627.1:c.713G>C
|
ENSP00000512066.1:n.713G>C
|
|
ENST00000695628.1:c.324G>C
|
ENSP00000512067.1:n.324G>C
|
|
ENST00000695629.1:c.205G>C
|
ENSP00000512068.1:p.Glu69Gln
|
|
ENST00000695630.1:c.492G>C
|
|
|
ENST00000695631.1:c.115-89G>C
|
|
|
ENST00000703407.1:c.1237G>C
|
ENSP00000512057.1:p.Glu413Gln
|
|
ENST00000308731.8:c.1765G>C
MANE Select
|
ENSP00000308176.8:p.Glu589Gln
|
|
ENST00000308731.7:c.1765G>C
|
ENSP00000308176.7:p.Glu589Gln
|
|
ENST00000372880.5:c.1237G>C
|
ENSP00000361971.1:p.Glu413Gln
|
|
ENST00000470069.1:n.130G>C
|
|
|
ENST00000488970.1:n.367G>C
|
|
|
ENST00000618050.4:c.1764G>C
|
ENSP00000479125.1:n.1764G>C
|
|
ENST00000621635.4:c.1867G>C
|
ENSP00000483570.1:p.Glu623Gln
|
|
NM_000061.2:c.1765G>C , LRG_128t1:c.1765G>C
|
NP_000052.1:p.Glu589Gln
|
|
NM_001287344.1:c.1867G>C
|
NP_001274273.1:p.Glu623Gln
|
|
NM_001287345.1:c.1237G>C
|
NP_001274274.1:p.Glu413Gln
|
|
NM_000061.3:c.1765G>C
MANE Select
|
NP_000052.1:p.Glu589Gln
|
|
NM_001287344.2:c.1867G>C
|
NP_001274273.1:p.Glu623Gln
|
|
NM_001287345.2:c.1237G>C
|
NP_001274274.1:p.Glu413Gln
|
|