ENST00000321264.9:c.1307-117C>A
MANE Select
|
ENSP00000315351.4:n.1307-117C>A
|
|
ENST00000321264.8:c.1307-117C>A
|
ENSP00000315351.4:n.1307-117C>A
|
|
ENST00000400769.6:c.*57-117C>A
|
ENSP00000383580.2:n.*57-117C>A
|
|
ENST00000403782.5:c.905-117C>A
|
ENSP00000384723.1:n.905-117C>A
|
|
ENST00000436747.5:c.*2543-117C>A
|
ENSP00000400212.1:n.*2543-117C>A
|
|
ENST00000445308.1:c.703-117C>A
|
|
|
ENST00000468064.5:n.1197-117C>A
|
|
|
ENST00000470343.5:n.788-117C>A
|
|
|
ENST00000473126.1:n.506-117C>A
|
|
|
ENST00000486953.5:n.1134-120C>A
|
|
|
ENST00000610344.1:c.*151-117C>A
|
ENSP00000481906.1:n.*151-117C>A
|
|
NM_001287249.1:c.905-117C>A
|
NP_001274178.1:n.905-117C>A
|
|
NM_152783.4:c.1307-117C>A
|
NP_689996.4:n.1307-117C>A
|
|
NR_109778.1:n.1229-117C>A
|
|
|
XM_011511734.1:c.1427-117C>A
|
XP_011510036.1:n.1427-117C>A
|
|
XM_011511735.1:c.1385-117C>A
|
XP_011510037.1:n.1385-117C>A
|
|
XM_011511736.1:c.1349-117C>A
|
XP_011510038.1:n.1349-117C>A
|
|
XM_011511744.1:c.*39-117C>A
|
XP_011510046.1:n.*39-117C>A
|
|
XM_011511750.1:c.1219-117C>A
|
XP_011510052.1:n.1219-117C>A
|
|
XM_011511754.1:c.866-117C>A
|
XP_011510056.1:n.866-117C>A
|
|
XM_011511755.1:c.857-117C>A
|
XP_011510057.1:n.857-117C>A
|
|
XM_011511756.1:c.854-117C>A
|
XP_011510058.1:n.854-117C>A
|
|
XR_923004.1:n.1939-117C>A
|
|
|
XR_923007.1:n.1649-117C>A
|
|
|
XR_923011.1:n.1750-117C>A
|
|
|
NM_001352824.1:c.746-117C>A
|
NP_001339753.1:n.746-117C>A
|
|
XM_011511734.2:c.1427-117C>A
|
XP_011510036.1:n.1427-117C>A
|
|
XM_011511735.2:c.1385-117C>A
|
XP_011510037.1:n.1385-117C>A
|
|
XM_011511736.2:c.1349-117C>A
|
XP_011510038.1:n.1349-117C>A
|
|
XM_011511744.2:c.*39-117C>A
|
XP_011510046.1:n.*39-117C>A
|
|
XM_011511750.3:c.1219-117C>A
|
XP_011510052.1:n.1219-117C>A
|
|
XM_011511756.2:c.854-117C>A
|
XP_011510058.1:n.854-117C>A
|
|
XM_024453102.1:c.1199-117C>A
|
XP_024308870.1:n.1199-117C>A
|
|
XR_001738918.2:n.1681-117C>A
|
|
|
XR_001738919.2:n.1615-117C>A
|
|
|
XR_923004.3:n.1938-117C>A
|
|
|
XR_923007.3:n.1648-117C>A
|
|
|
XR_923011.3:n.1749-117C>A
|
|
|
NM_152783.5:c.1307-117C>A
MANE Select
|
NP_689996.4:n.1307-117C>A
|
|
NM_001287249.2:c.905-117C>A
|
NP_001274178.1:n.905-117C>A
|
|
NM_001352824.2:c.746-117C>A
|
NP_001339753.1:n.746-117C>A
|
|
NR_109778.2:n.1178-117C>A
|
|
|