ENST00000302250.7:c.1336A>T
(FAM151A)
MANE Select
|
ENSP00000306888.2:p.Lys446Ter
|
|
ENST00000343744.7:c.*578T>A
(ACOT11)
MANE Select
|
ENSP00000340260.2:n.*578T>A
|
|
ENST00000302250.6:c.1336A>T
(FAM151A)
|
ENSP00000306888.2:p.Lys446Ter
|
|
ENST00000343744.6:c.*578T>A
(ACOT11)
|
ENSP00000340260.2:n.*578T>A
|
|
ENST00000371304.2:c.918-143A>T
(FAM151A)
|
ENSP00000360353.2:n.918-143A>T
|
|
ENST00000371316.3:c.1629+1622T>A
(ACOT11)
|
ENSP00000360366.3:n.1629+1622T>A
|
|
ENST00000481208.5:n.2441T>A
(ACOT11)
|
|
|
NM_015547.3:c.1629+1622T>A
(ACOT11)
|
NP_056362.1:n.1629+1622T>A
|
|
NM_147161.3:c.*578T>A
(ACOT11)
|
NP_671517.1:n.*578T>A
|
|
NM_176782.2:c.1336A>T
(FAM151A)
|
NP_788954.2:p.Lys446Ter
|
|
XM_006710599.2:c.1258A>T
(FAM151A)
|
XP_006710662.1:p.Lys420Ter
|
|
XM_006710599.3:c.1258A>T
(FAM151A)
|
XP_006710662.1:p.Lys420Ter
|
|
NM_176782.3:c.1336A>T
(FAM151A)
MANE Select
|
NP_788954.2:p.Lys446Ter
|
|
NM_015547.4:c.1629+1622T>A
(ACOT11)
|
NP_056362.1:n.1629+1622T>A
|
|
NM_147161.4:c.*578T>A
(ACOT11)
MANE Select
|
NP_671517.1:n.*578T>A
|
|