ENST00000246957.10:c.37C>T
MANE Select
|
ENSP00000246957.5:p.Arg13Cys
|
|
ENST00000246957.9:c.37C>T
|
ENSP00000246957.5:p.Arg13Cys
|
|
ENST00000538171.5:c.37C>T
|
ENSP00000442070.1:p.Arg13Cys
|
|
ENST00000570403.1:c.37C>T
|
ENSP00000461354.1:p.Arg13Cys
|
|
ENST00000571011.1:c.37C>T
|
ENSP00000460545.1:p.Arg13Cys
|
|
ENST00000571804.5:c.37C>T
|
ENSP00000461618.1:p.Arg13Cys
|
|
ENST00000574941.5:n.55C>T
|
|
|
ENST00000576106.5:n.82C>T
|
|
|
NM_001272049.1:c.37C>T
|
NP_001258978.1:p.Arg13Cys
|
|
NM_016292.2:c.37C>T
|
NP_057376.2:p.Arg13Cys
|
|
NM_016292.3:c.37C>T
MANE Select
|
NP_057376.2:p.Arg13Cys
|
|
NM_001272049.2:c.37C>T
|
NP_001258978.1:p.Arg13Cys
|
|