ENST00000302250.7:c.*57A>C
(FAM151A)
MANE Select
|
ENSP00000306888.2:n.*57A>C
|
|
ENST00000343744.7:c.*99T>G
(ACOT11)
MANE Select
|
ENSP00000340260.2:n.*99T>G
|
|
ENST00000302250.6:c.*57A>C
(FAM151A)
|
ENSP00000306888.2:n.*57A>C
|
|
ENST00000343744.6:c.*99T>G
(ACOT11)
|
ENSP00000340260.2:n.*99T>G
|
|
ENST00000371304.2:c.*57A>C
(FAM151A)
|
ENSP00000360353.2:n.*57A>C
|
|
ENST00000371316.3:c.1629+1143T>G
(ACOT11)
|
ENSP00000360366.3:n.1629+1143T>G
|
|
ENST00000481208.5:n.1962T>G
(ACOT11)
|
|
|
NM_015547.3:c.1629+1143T>G
(ACOT11)
|
NP_056362.1:n.1629+1143T>G
|
|
NM_147161.3:c.*99T>G
(ACOT11)
|
NP_671517.1:n.*99T>G
|
|
NM_176782.2:c.*57A>C
(FAM151A)
|
NP_788954.2:n.*57A>C
|
|
XM_006710599.2:c.*57A>C
(FAM151A)
|
XP_006710662.1:n.*57A>C
|
|
XM_006710599.3:c.*57A>C
(FAM151A)
|
XP_006710662.1:n.*57A>C
|
|
NM_176782.3:c.*57A>C
(FAM151A)
MANE Select
|
NP_788954.2:n.*57A>C
|
|
NM_015547.4:c.1629+1143T>G
(ACOT11)
|
NP_056362.1:n.1629+1143T>G
|
|
NM_147161.4:c.*99T>G
(ACOT11)
MANE Select
|
NP_671517.1:n.*99T>G
|
|