ENST00000366159.9:n.1701G>T
|
|
|
ENST00000437813.8:c.*61G>T
|
ENSP00000513672.1:n.*61G>T
|
|
ENST00000440083.7:c.819G>T
|
ENSP00000413224.3:p.Glu273Asp
|
|
ENST00000535038.2:n.782G>T
|
|
|
ENST00000535958.2:c.*427G>T
|
ENSP00000513673.1:n.*427G>T
|
|
ENST00000698337.1:n.449G>T
|
|
|
ENST00000698338.1:n.873G>T
|
|
|
ENST00000698339.1:c.*95G>T
|
ENSP00000513670.1:n.*95G>T
|
|
ENST00000698340.1:c.552-167G>T
|
ENSP00000513671.1:n.552-167G>T
|
|
ENST00000162749.7:c.600G>T
MANE Select
|
ENSP00000162749.2:p.Glu200Asp
|
|
ENST00000162749.6:c.600G>T
|
ENSP00000162749.2:p.Glu200Asp
|
|
ENST00000534885.5:c.*77G>T
|
ENSP00000441803.1:n.*77G>T
|
|
ENST00000535038.1:n.270G>T
|
|
|
ENST00000536717.5:n.504G>T
|
|
|
ENST00000537842.5:n.204G>T
|
|
|
ENST00000539372.5:c.600G>T
|
ENSP00000442059.1:p.Glu200Asp
|
|
ENST00000540022.5:c.471G>T
|
ENSP00000438343.1:p.Glu157Asp
|
|
ENST00000543359.5:n.38-167G>T
|
|
|
ENST00000543995.5:c.*187G>T
|
ENSP00000442405.1:n.*187G>T
|
|
NM_001065.3:c.600G>T , LRG_193t1:c.600G>T
|
NP_001056.1:p.Glu200Asp
|
|
NM_001346091.1:c.276G>T
|
NP_001333020.1:p.Glu92Asp
|
|
NM_001346092.1:c.141G>T
|
NP_001333021.1:p.Glu47Asp
|
|
NR_144351.1:n.855-167G>T
|
|
|
NM_001065.4:c.600G>T
MANE Select
|
NP_001056.1:p.Glu200Asp
|
|
NM_001346091.2:c.276G>T
|
NP_001333020.1:p.Glu92Asp
|
|
NM_001346092.2:c.141G>T
|
NP_001333021.1:p.Glu47Asp
|
|
NR_144351.2:n.814-167G>T
|
|
|