ENST00000263967.4:c.3057T>A
MANE Select
|
ENSP00000263967.3:p.Ile1019=
|
|
ENST00000462255.2:n.2080T>A
|
|
|
ENST00000643187.1:c.*137T>A
|
ENSP00000493507.1:n.*137T>A
|
|
ENST00000674534.1:n.3965T>A
|
|
|
ENST00000674622.1:c.1478T>A
|
ENSP00000502417.1:n.1478T>A
|
|
ENST00000675467.1:n.5864T>A
|
|
|
ENST00000675786.1:c.*1624T>A
|
ENSP00000502323.1:n.*1624T>A
|
|
ENST00000675796.1:n.2952T>A
|
|
|
ENST00000263967.3:c.3057T>A
|
ENSP00000263967.3:p.Ile1019=
|
|
NM_006218.2:c.3057T>A , LRG_310t1:c.3057T>A
|
NP_006209.2:p.Ile1019=
|
|
XM_006713658.2:c.3057T>A
|
XP_006713721.1:p.Ile1019=
|
|
XM_011512894.1:c.3057T>A
|
XP_011511196.1:p.Ile1019=
|
|
NM_006218.3:c.3057T>A
|
NP_006209.2:p.Ile1019=
|
|
XM_006713658.4:c.3057T>A
|
XP_006713721.1:p.Ile1019=
|
|
XM_011512894.2:c.3057T>A
|
XP_011511196.1:p.Ile1019=
|
|
NM_006218.4:c.3057T>A
MANE Select
|
NP_006209.2:p.Ile1019=
|
|