ENST00000300452.8:c.421C>A
MANE Select
|
ENSP00000300452.3:p.Arg141=
|
|
ENST00000300452.7:c.421C>A
|
ENSP00000300452.3:p.Arg141=
|
|
ENST00000461102.1:n.1760C>A
|
|
|
NM_001305942.1:c.*3-1303C>A
|
NP_001292871.1:n.*3-1303C>A
|
|
NM_016035.3:c.421C>A
|
NP_057119.2:p.Arg141=
|
|
NM_016035.4:c.421C>A
|
NP_057119.2:p.Arg141=
|
|
XR_929805.1:n.749-679C>A
|
|
|
XM_017014792.1:c.*3-679C>A
|
XP_016870281.1:n.*3-679C>A
|
|
XR_001746316.2:n.674C>A
|
|
|
XR_929805.3:n.749-679C>A
|
|
|
NM_016035.5:c.421C>A
MANE Select
|
NP_057119.3:p.Arg141=
|
|
NM_001305942.2:c.*3-1303C>A
|
NP_001292871.2:n.*3-1303C>A
|
|