ENST00000272895.12:c.*258A>G
(ABCA12)
MANE Select
|
ENSP00000272895.7:n.*258A>G
|
|
ENST00000272895.11:c.*258A>G
(ABCA12)
|
ENSP00000272895.7:n.*258A>G
|
|
NM_015657.3:c.*258A>G
(ABCA12)
|
NP_056472.2:n.*258A>G
|
|
NM_173076.2:c.*258A>G
(ABCA12)
|
NP_775099.2:n.*258A>G
|
|
NR_103740.1:n.8346A>G
(ABCA12)
|
|
|
NR_110292.1:n.322-15449T>C
(SNHG31)
|
|
|
XM_011510951.1:c.*258A>G
(ABCA12)
|
XP_011509253.1:n.*258A>G
|
|
XM_011510951.2:c.*258A>G
(ABCA12)
|
XP_011509253.1:n.*258A>G
|
|
NM_173076.3:c.*258A>G
(ABCA12)
MANE Select
|
NP_775099.2:n.*258A>G
|
|
NR_103740.2:n.8544A>G
(ABCA12)
|
|
|
NM_015657.4:c.*258A>G
(ABCA12)
|
NP_056472.2:n.*258A>G
|
|