ENST00000302250.7:c.1420_1474del
(FAM151A)
MANE Select
|
ENSP00000306888.2:p.Val474SerfsTer7
|
|
ENST00000343744.7:c.*442_*496del
(ACOT11)
MANE Select
|
ENSP00000340260.2:n.*442_*496del
|
|
ENST00000302250.6:c.1420_1474del
(FAM151A)
|
ENSP00000306888.2:p.Val474SerfsTer7
|
|
ENST00000343744.6:c.*442_*496del
(ACOT11)
|
ENSP00000340260.2:n.*442_*496del
|
|
ENST00000371304.2:c.918-59_918-5del
(FAM151A)
|
ENSP00000360353.2:n.918-59_918-5del
|
|
ENST00000371316.3:c.1629+1486_1629+1540del
(ACOT11)
|
ENSP00000360366.3:n.1629+1486_1629+1540del
|
|
ENST00000481208.5:n.2305_2359del
(ACOT11)
|
|
|
NM_015547.3:c.1629+1486_1629+1540del
(ACOT11)
|
NP_056362.1:n.1629+1486_1629+1540del
|
|
NM_147161.3:c.*442_*496del
(ACOT11)
|
NP_671517.1:n.*442_*496del
|
|
NM_176782.2:c.1420_1474del
(FAM151A)
|
NP_788954.2:p.Val474SerfsTer7
|
|
XM_006710599.2:c.1342_1396del
(FAM151A)
|
XP_006710662.1:p.Val448SerfsTer7
|
|
XM_006710599.3:c.1342_1396del
(FAM151A)
|
XP_006710662.1:p.Val448SerfsTer7
|
|
NM_176782.3:c.1420_1474del
(FAM151A)
MANE Select
|
NP_788954.2:p.Val474SerfsTer7
|
|
NM_015547.4:c.1629+1486_1629+1540del
(ACOT11)
|
NP_056362.1:n.1629+1486_1629+1540del
|
|
NM_147161.4:c.*442_*496del
(ACOT11)
MANE Select
|
NP_671517.1:n.*442_*496del
|
|