ENST00000366159.9:n.261G>T
|
|
|
ENST00000437813.8:c.227G>T
|
ENSP00000513672.1:p.Gly76Val
|
|
ENST00000440083.7:c.227G>T
|
ENSP00000413224.3:p.Gly76Val
|
|
ENST00000535958.2:c.*54G>T
|
ENSP00000513673.1:n.*54G>T
|
|
ENST00000698339.1:c.227G>T
|
ENSP00000513670.1:p.Gly76Val
|
|
ENST00000698340.1:c.227G>T
|
ENSP00000513671.1:p.Gly76Val
|
|
ENST00000162749.7:c.227G>T
MANE Select
|
ENSP00000162749.2:p.Gly76Val
|
|
ENST00000162749.6:c.227G>T
|
ENSP00000162749.2:p.Gly76Val
|
|
ENST00000366159.8:c.227G>T
|
ENSP00000380389.3:p.Gly76Val
|
|
ENST00000437813.7:n.188G>T
|
|
|
ENST00000440083.6:c.227G>T
|
ENSP00000413224.2:p.Gly76Val
|
|
ENST00000534885.5:c.73G>T
|
ENSP00000441803.1:p.Gly25Cys
|
|
ENST00000535958.1:n.473G>T
|
|
|
ENST00000536194.1:c.200G>T
|
ENSP00000442919.1:p.Gly67Val
|
|
ENST00000539372.5:c.227G>T
|
ENSP00000442059.1:p.Gly76Val
|
|
ENST00000540022.5:c.193+259G>T
|
ENSP00000438343.1:n.193+259G>T
|
|
ENST00000543048.5:c.214+13G>T
|
ENSP00000439981.1:n.214+13G>T
|
|
ENST00000543995.5:c.193+259G>T
|
ENSP00000442405.1:n.193+259G>T
|
|
NM_001065.3:c.227G>T , LRG_193t1:c.227G>T
|
NP_001056.1:p.Gly76Val
|
|
NM_001346091.1:c.-98G>T
|
NP_001333020.1:n.-98G>T
|
|
NM_001346092.1:c.-351G>T
|
NP_001333021.1:n.-351G>T
|
|
NR_144351.1:n.530G>T
|
|
|
NM_001065.4:c.227G>T
MANE Select
|
NP_001056.1:p.Gly76Val
|
|
NM_001346091.2:c.-98G>T
|
NP_001333020.1:n.-98G>T
|
|
NM_001346092.2:c.-351G>T
|
NP_001333021.1:n.-351G>T
|
|
NR_144351.2:n.489G>T
|
|
|