ENST00000266771.10:c.587A>T
MANE Select
|
ENSP00000266771.5:p.Asn196Ile
|
|
ENST00000266771.9:c.587A>T
|
ENSP00000266771.5:p.Asn196Ile
|
|
ENST00000366292.6:n.899A>T
|
|
|
ENST00000376740.8:c.166A>T
|
|
|
ENST00000376744.8:c.423A>T
|
|
|
ENST00000535272.1:n.381A>T
|
|
|
ENST00000539703.1:n.237A>T
|
|
|
NM_145648.3:c.587A>T
|
NP_663623.1:p.Asn196Ile
|
|
XM_011537895.1:c.737A>T
|
XP_011536197.1:p.Asn246Ile
|
|
XR_429081.2:n.610A>T
|
|
|
XR_944494.1:n.760A>T
|
|
|
XR_944495.1:n.760A>T
|
|
|
XR_944496.1:n.760A>T
|
|
|
XR_944497.1:n.760A>T
|
|
|
XM_017018791.1:c.737A>T
|
XP_016874280.1:p.Asn246Ile
|
|
XM_017018792.1:c.737A>T
|
XP_016874281.1:p.Asn246Ile
|
|
XM_017018793.1:c.587A>T
|
XP_016874282.1:p.Asn196Ile
|
|
XR_002957287.1:n.610A>T
|
|
|
XR_944496.2:n.760A>T
|
|
|
NM_145648.4:c.587A>T
MANE Select
|
NP_663623.1:p.Asn196Ile
|
|