ENST00000682338.1:c.1227+150T>G
|
ENSP00000507062.1:n.1227+150T>G
|
|
ENST00000682793.1:c.1227+150T>G
|
ENSP00000506910.1:n.1227+150T>G
|
|
ENST00000682838.1:c.*969+150T>G
|
ENSP00000507652.1:n.*969+150T>G
|
|
ENST00000683578.1:c.1227+150T>G
|
ENSP00000507430.1:n.1227+150T>G
|
|
ENST00000683606.1:n.842+150T>G
|
|
|
ENST00000683661.1:n.2762+150T>G
|
|
|
ENST00000684324.1:c.1227+150T>G
|
ENSP00000507937.1:n.1227+150T>G
|
|
ENST00000684545.1:c.1227+150T>G
|
ENSP00000506733.1:n.1227+150T>G
|
|
ENST00000684624.1:n.604+150T>G
|
|
|
ENST00000684714.1:c.1227+150T>G
|
ENSP00000506861.1:n.1227+150T>G
|
|
ENST00000684731.1:n.688+150T>G
|
|
|
ENST00000375679.9:c.1227+150T>G
MANE Select
|
ENSP00000364831.5:n.1227+150T>G
|
|
ENST00000375667.7:c.720+150T>G
|
ENSP00000364819.3:n.720+150T>G
|
|
ENST00000375679.8:c.1227+150T>G
|
ENSP00000364831.4:n.1227+150T>G
|
|
ENST00000619181.4:c.846+150T>G
|
ENSP00000483866.1:n.846+150T>G
|
|
NM_000085.4:c.1227+150T>G
|
NP_000076.2:n.1227+150T>G
|
|
NM_001165945.2:c.720+150T>G
|
NP_001159417.2:n.720+150T>G
|
|
XM_011540619.1:c.1068+150T>G
|
XP_011538921.1:n.1068+150T>G
|
|
XM_011540620.1:c.1227+150T>G
|
XP_011538922.1:n.1227+150T>G
|
|
XM_011540621.1:c.576+150T>G
|
XP_011538923.1:n.576+150T>G
|
|
NM_000085.5:c.1227+150T>G
MANE Select
|
NP_000076.2:n.1227+150T>G
|
|