ENST00000263967.4:c.3156A>G
MANE Select
|
ENSP00000263967.3:p.Thr1052=
|
|
ENST00000462255.2:n.2179A>G
|
|
|
ENST00000643187.1:c.*236A>G
|
ENSP00000493507.1:n.*236A>G
|
|
ENST00000674534.1:n.4064A>G
|
|
|
ENST00000674622.1:c.1577A>G
|
ENSP00000502417.1:n.1577A>G
|
|
ENST00000675467.1:n.5963A>G
|
|
|
ENST00000675786.1:c.*1723A>G
|
ENSP00000502323.1:n.*1723A>G
|
|
ENST00000675796.1:n.3051A>G
|
|
|
ENST00000263967.3:c.3156A>G
|
ENSP00000263967.3:p.Thr1052=
|
|
NM_006218.2:c.3156A>G , LRG_310t1:c.3156A>G
|
NP_006209.2:p.Thr1052=
|
|
XM_006713658.2:c.3156A>G
|
XP_006713721.1:p.Thr1052=
|
|
XM_011512894.1:c.3156A>G
|
XP_011511196.1:p.Thr1052=
|
|
NM_006218.3:c.3156A>G
|
NP_006209.2:p.Thr1052=
|
|
XM_006713658.4:c.3156A>G
|
XP_006713721.1:p.Thr1052=
|
|
XM_011512894.2:c.3156A>G
|
XP_011511196.1:p.Thr1052=
|
|
NM_006218.4:c.3156A>G
MANE Select
|
NP_006209.2:p.Thr1052=
|
|