ENST00000263967.4:c.*5A>T
MANE Select
|
ENSP00000263967.3:n.*5A>T
|
|
ENST00000462255.2:n.2235A>T
|
|
|
ENST00000643187.1:c.*292A>T
|
ENSP00000493507.1:n.*292A>T
|
|
ENST00000674534.1:n.4120A>T
|
|
|
ENST00000674622.1:c.1633A>T
|
ENSP00000502417.1:n.1633A>T
|
|
ENST00000675467.1:n.6019A>T
|
|
|
ENST00000675786.1:c.*1779A>T
|
ENSP00000502323.1:n.*1779A>T
|
|
ENST00000675796.1:n.3107A>T
|
|
|
ENST00000263967.3:c.*5A>T
|
ENSP00000263967.3:n.*5A>T
|
|
NM_006218.2:c.*5A>T , LRG_310t1:c.*5A>T
|
NP_006209.2:n.*5A>T
|
|
XM_006713658.2:c.*5A>T
|
XP_006713721.1:n.*5A>T
|
|
XM_011512894.1:c.*5A>T
|
XP_011511196.1:n.*5A>T
|
|
NM_006218.3:c.*5A>T
|
NP_006209.2:n.*5A>T
|
|
XM_006713658.4:c.*5A>T
|
XP_006713721.1:n.*5A>T
|
|
XM_011512894.2:c.*5A>T
|
XP_011511196.1:n.*5A>T
|
|
NM_006218.4:c.*5A>T
MANE Select
|
NP_006209.2:n.*5A>T
|
|