ENST00000297770.10:c.838+1G>A
(CPA6)
MANE Select
|
ENSP00000297770.4:n.838+1G>A
|
|
ENST00000638254.1:c.*434+1G>A
(CPA6)
|
ENSP00000491129.1:n.*434+1G>A
|
|
ENST00000297770.8:c.838+1G>A
(CPA6)
|
ENSP00000297770.4:n.838+1G>A
|
|
ENST00000479862.6:c.*434+1G>A
(CPA6)
|
ENSP00000419016.2:n.*434+1G>A
|
|
ENST00000518549.1:c.839G>A
(CPA6)
|
ENSP00000431112.1:p.Gly280Asp
|
|
NM_020361.4:c.838+1G>A
(CPA6)
|
NP_065094.3:n.838+1G>A
|
|
XM_011517569.1:c.931+1G>A
(CPA6)
|
XP_011515871.1:n.931+1G>A
|
|
XM_011517570.1:c.394+1G>A
(CPA6)
|
XP_011515872.1:n.394+1G>A
|
|
NR_136224.1:n.694-7198C>T
(ARFGEF1-DT)
|
|
|
XM_011517570.2:c.394+1G>A
(CPA6)
|
XP_011515872.1:n.394+1G>A
|
|
XM_017013646.1:c.394+1G>A
(CPA6)
|
XP_016869135.1:n.394+1G>A
|
|
XR_001745565.1:n.1646+1G>A
(CPA6)
|
|
|
NM_020361.5:c.838+1G>A
(CPA6)
MANE Select
|
NP_065094.3:n.838+1G>A
|
|