ENST00000394975.3:c.392T>A
MANE Select
|
ENSP00000378426.2:p.Phe131Tyr
|
|
ENST00000300851.10:c.*3T>A
|
ENSP00000300851.6:n.*3T>A
|
|
ENST00000319788.11:c.*3T>A
|
ENSP00000326135.7:n.*3T>A
|
|
ENST00000354895.4:c.*3T>A
|
ENSP00000346969.4:n.*3T>A
|
|
ENST00000394971.7:c.*3T>A
|
ENSP00000378422.3:n.*3T>A
|
|
ENST00000394975.2:c.392T>A
|
ENSP00000378426.2:p.Phe131Tyr
|
|
ENST00000420057.2:c.354T>A
|
|
|
ENST00000472468.1:c.77T>A
|
ENSP00000458994.1:p.Phe26Tyr
|
|
ENST00000498155.1:c.*3T>A
|
ENSP00000417662.1:n.*3T>A
|
|
ENST00000529564.1:c.283+2078T>A
|
ENSP00000431371.1:n.283+2078T>A
|
|
ENST00000532364.1:c.173+3323T>A
|
ENSP00000460316.1:n.173+3323T>A
|
|
ENST00000533518.5:c.265T>A
|
|
|
NM_001311311.1:c.476T>A
|
NP_001298240.1:p.Phe159Tyr
|
|
NM_024006.4:c.392T>A
|
NP_076869.1:p.Phe131Tyr
|
|
NM_024006.5:c.392T>A
|
NP_076869.1:p.Phe131Tyr
|
|
NM_206824.1:c.*3T>A
|
NP_996560.1:n.*3T>A
|
|
NM_206824.2:c.*3T>A
|
NP_996560.1:n.*3T>A
|
|
XM_011545944.1:c.392T>A
|
XP_011544246.1:p.Phe131Tyr
|
|
XM_011545945.1:c.*3T>A
|
XP_011544247.1:n.*3T>A
|
|
XR_950848.1:n.1180T>A
|
|
|
NM_024006.6:c.392T>A
MANE Select
|
NP_076869.1:p.Phe131Tyr
|
|
NM_001311311.2:c.476T>A
|
NP_001298240.1:p.Phe159Tyr
|
|
NM_206824.3:c.*3T>A
|
NP_996560.1:n.*3T>A
|
|