ENST00000297770.10:c.838+7T>G
(CPA6)
MANE Select
|
ENSP00000297770.4:n.838+7T>G
|
|
ENST00000638254.1:c.*434+7T>G
(CPA6)
|
ENSP00000491129.1:n.*434+7T>G
|
|
ENST00000297770.8:c.838+7T>G
(CPA6)
|
ENSP00000297770.4:n.838+7T>G
|
|
ENST00000479862.6:c.*434+7T>G
(CPA6)
|
ENSP00000419016.2:n.*434+7T>G
|
|
ENST00000518549.1:c.845T>G
(CPA6)
|
ENSP00000431112.1:p.Phe282Cys
|
|
NM_020361.4:c.838+7T>G
(CPA6)
|
NP_065094.3:n.838+7T>G
|
|
XM_011517569.1:c.931+7T>G
(CPA6)
|
XP_011515871.1:n.931+7T>G
|
|
XM_011517570.1:c.394+7T>G
(CPA6)
|
XP_011515872.1:n.394+7T>G
|
|
NR_136224.1:n.694-7204A>C
(ARFGEF1-DT)
|
|
|
XM_011517570.2:c.394+7T>G
(CPA6)
|
XP_011515872.1:n.394+7T>G
|
|
XM_017013646.1:c.394+7T>G
(CPA6)
|
XP_016869135.1:n.394+7T>G
|
|
XR_001745565.1:n.1646+7T>G
(CPA6)
|
|
|
NM_020361.5:c.838+7T>G
(CPA6)
MANE Select
|
NP_065094.3:n.838+7T>G
|
|