ENST00000464006.2:n.671A>T
|
|
|
ENST00000478995.2:n.1051A>T
|
|
|
ENST00000488970.2:n.1049A>T
|
|
|
ENST00000695614.1:c.891A>T
|
ENSP00000512053.1:p.Gln297His
|
|
ENST00000695615.1:c.891A>T
|
ENSP00000512054.1:p.Gln297His
|
|
ENST00000695616.1:c.*736A>T
|
ENSP00000512055.1:n.*736A>T
|
|
ENST00000695617.1:c.888A>T
|
ENSP00000512056.1:p.Gln296His
|
|
ENST00000695618.1:c.*640A>T
|
ENSP00000512058.1:n.*640A>T
|
|
ENST00000695619.1:c.*684+792A>T
|
ENSP00000512059.1:n.*684+792A>T
|
|
ENST00000695620.1:c.*736A>T
|
ENSP00000512060.1:n.*736A>T
|
|
ENST00000695621.1:c.891A>T
|
ENSP00000512061.1:p.Gln297His
|
|
ENST00000695622.1:c.828A>T
|
ENSP00000512062.1:p.Gln276His
|
|
ENST00000695623.1:c.885A>T
|
ENSP00000512063.1:p.Gln295His
|
|
ENST00000695624.1:n.196A>T
|
|
|
ENST00000695625.1:c.891A>T
|
ENSP00000512064.1:p.Gln297His
|
|
ENST00000703407.1:c.891A>T
|
ENSP00000512057.1:p.Gln297His
|
|
ENST00000308731.8:c.891A>T
MANE Select
|
ENSP00000308176.8:p.Gln297His
|
|
ENST00000308731.7:c.891A>T
|
ENSP00000308176.7:p.Gln297His
|
|
ENST00000372880.5:c.891A>T
|
ENSP00000361971.1:p.Gln297His
|
|
ENST00000618050.4:c.891A>T
|
ENSP00000479125.1:p.Gln297His
|
|
ENST00000621635.4:c.993A>T
|
ENSP00000483570.1:p.Gln331His
|
|
NM_000061.2:c.891A>T , LRG_128t1:c.891A>T
|
NP_000052.1:p.Gln297His
|
|
NM_001287344.1:c.993A>T
|
NP_001274273.1:p.Gln331His
|
|
NM_001287345.1:c.891A>T
|
NP_001274274.1:p.Gln297His
|
|
NM_000061.3:c.891A>T
MANE Select
|
NP_000052.1:p.Gln297His
|
|
NM_001287344.2:c.993A>T
|
NP_001274273.1:p.Gln331His
|
|
NM_001287345.2:c.891A>T
|
NP_001274274.1:p.Gln297His
|
|