ENST00000302250.7:c.1345C>A
(FAM151A)
MANE Select
|
ENSP00000306888.2:p.His449Asn
|
|
ENST00000343744.7:c.*569G>T
(ACOT11)
MANE Select
|
ENSP00000340260.2:n.*569G>T
|
|
ENST00000302250.6:c.1345C>A
(FAM151A)
|
ENSP00000306888.2:p.His449Asn
|
|
ENST00000343744.6:c.*569G>T
(ACOT11)
|
ENSP00000340260.2:n.*569G>T
|
|
ENST00000371304.2:c.918-134C>A
(FAM151A)
|
ENSP00000360353.2:n.918-134C>A
|
|
ENST00000371316.3:c.1629+1613G>T
(ACOT11)
|
ENSP00000360366.3:n.1629+1613G>T
|
|
ENST00000481208.5:n.2432G>T
(ACOT11)
|
|
|
NM_015547.3:c.1629+1613G>T
(ACOT11)
|
NP_056362.1:n.1629+1613G>T
|
|
NM_147161.3:c.*569G>T
(ACOT11)
|
NP_671517.1:n.*569G>T
|
|
NM_176782.2:c.1345C>A
(FAM151A)
|
NP_788954.2:p.His449Asn
|
|
XM_006710599.2:c.1267C>A
(FAM151A)
|
XP_006710662.1:p.His423Asn
|
|
XM_006710599.3:c.1267C>A
(FAM151A)
|
XP_006710662.1:p.His423Asn
|
|
NM_176782.3:c.1345C>A
(FAM151A)
MANE Select
|
NP_788954.2:p.His449Asn
|
|
NM_015547.4:c.1629+1613G>T
(ACOT11)
|
NP_056362.1:n.1629+1613G>T
|
|
NM_147161.4:c.*569G>T
(ACOT11)
MANE Select
|
NP_671517.1:n.*569G>T
|
|