ENST00000272895.12:c.6569T>C
(ABCA12)
MANE Select
|
ENSP00000272895.7:p.Phe2190Ser
|
|
ENST00000272895.11:c.6569T>C
(ABCA12)
|
ENSP00000272895.7:p.Phe2190Ser
|
|
ENST00000389661.4:c.5615T>C
(ABCA12)
|
ENSP00000374312.4:p.Phe1872Ser
|
|
NM_015657.3:c.5615T>C
(ABCA12)
|
NP_056472.2:p.Phe1872Ser
|
|
NM_173076.2:c.6569T>C
(ABCA12)
|
NP_775099.2:p.Phe2190Ser
|
|
NR_103740.1:n.6869T>C
(ABCA12)
|
|
|
NR_110292.1:n.444+5985A>G
(SNHG31)
|
|
|
XM_011510951.1:c.6578T>C
(ABCA12)
|
XP_011509253.1:p.Phe2193Ser
|
|
XM_011510951.2:c.6578T>C
(ABCA12)
|
XP_011509253.1:p.Phe2193Ser
|
|
NM_173076.3:c.6569T>C
(ABCA12)
MANE Select
|
NP_775099.2:p.Phe2190Ser
|
|
NR_103740.2:n.7067T>C
(ABCA12)
|
|
|
NM_015657.4:c.5615T>C
(ABCA12)
|
NP_056472.2:p.Phe1872Ser
|
|