ENST00000272895.12:c.7718A>C
(ABCA12)
MANE Select
|
ENSP00000272895.7:p.Glu2573Ala
|
|
ENST00000272895.11:c.7718A>C
(ABCA12)
|
ENSP00000272895.7:p.Glu2573Ala
|
|
ENST00000389661.4:c.6764A>C
(ABCA12)
|
ENSP00000374312.4:p.Glu2255Ala
|
|
NM_015657.3:c.6764A>C
(ABCA12)
|
NP_056472.2:p.Glu2255Ala
|
|
NM_173076.2:c.7718A>C
(ABCA12)
|
NP_775099.2:p.Glu2573Ala
|
|
NR_103740.1:n.8018A>C
(ABCA12)
|
|
|
NR_110292.1:n.322-15121T>G
(SNHG31)
|
|
|
XM_011510951.1:c.7727A>C
(ABCA12)
|
XP_011509253.1:p.Glu2576Ala
|
|
XM_011510951.2:c.7727A>C
(ABCA12)
|
XP_011509253.1:p.Glu2576Ala
|
|
NM_173076.3:c.7718A>C
(ABCA12)
MANE Select
|
NP_775099.2:p.Glu2573Ala
|
|
NR_103740.2:n.8216A>C
(ABCA12)
|
|
|
NM_015657.4:c.6764A>C
(ABCA12)
|
NP_056472.2:p.Glu2255Ala
|
|