ENST00000272895.12:c.*191T>A
(ABCA12)
MANE Select
|
ENSP00000272895.7:n.*191T>A
|
|
ENST00000272895.11:c.*191T>A
(ABCA12)
|
ENSP00000272895.7:n.*191T>A
|
|
NM_015657.3:c.*191T>A
(ABCA12)
|
NP_056472.2:n.*191T>A
|
|
NM_173076.2:c.*191T>A
(ABCA12)
|
NP_775099.2:n.*191T>A
|
|
NR_103740.1:n.8279T>A
(ABCA12)
|
|
|
NR_110292.1:n.322-15382A>T
(SNHG31)
|
|
|
XM_011510951.1:c.*191T>A
(ABCA12)
|
XP_011509253.1:n.*191T>A
|
|
XM_011510951.2:c.*191T>A
(ABCA12)
|
XP_011509253.1:n.*191T>A
|
|
NM_173076.3:c.*191T>A
(ABCA12)
MANE Select
|
NP_775099.2:n.*191T>A
|
|
NR_103740.2:n.8477T>A
(ABCA12)
|
|
|
NM_015657.4:c.*191T>A
(ABCA12)
|
NP_056472.2:n.*191T>A
|
|