ENST00000266771.10:c.782T>A
MANE Select
|
ENSP00000266771.5:p.Phe261Tyr
|
|
ENST00000266771.9:c.782T>A
|
ENSP00000266771.5:p.Phe261Tyr
|
|
ENST00000366292.6:n.1094T>A
|
|
|
ENST00000376740.8:c.361T>A
|
|
|
ENST00000376744.8:c.618T>A
|
|
|
ENST00000539703.1:n.432T>A
|
|
|
ENST00000614634.1:c.-61T>A
|
ENSP00000483143.1:n.-61T>A
|
|
NM_145648.3:c.782T>A
|
NP_663623.1:p.Phe261Tyr
|
|
XM_011537895.1:c.932T>A
|
XP_011536197.1:p.Phe311Tyr
|
|
XR_429081.2:n.805T>A
|
|
|
XR_944494.1:n.955T>A
|
|
|
XR_944495.1:n.955T>A
|
|
|
XR_944496.1:n.955T>A
|
|
|
XR_944497.1:n.955T>A
|
|
|
XM_017018791.1:c.932T>A
|
XP_016874280.1:p.Phe311Tyr
|
|
XM_017018792.1:c.932T>A
|
XP_016874281.1:p.Phe311Tyr
|
|
XM_017018793.1:c.782T>A
|
XP_016874282.1:p.Phe261Tyr
|
|
XR_002957287.1:n.805T>A
|
|
|
XR_944496.2:n.955T>A
|
|
|
NM_145648.4:c.782T>A
MANE Select
|
NP_663623.1:p.Phe261Tyr
|
|