ENST00000297770.10:c.777G>T
(CPA6)
MANE Select
|
ENSP00000297770.4:p.Arg259Ser
|
|
ENST00000638254.1:c.*373G>T
(CPA6)
|
ENSP00000491129.1:n.*373G>T
|
|
ENST00000297770.8:c.777G>T
(CPA6)
|
ENSP00000297770.4:p.Arg259Ser
|
|
ENST00000479862.6:c.*373G>T
(CPA6)
|
ENSP00000419016.2:n.*373G>T
|
|
ENST00000518549.1:c.777G>T
(CPA6)
|
ENSP00000431112.1:p.Arg259Ser
|
|
NM_020361.4:c.777G>T
(CPA6)
|
NP_065094.3:p.Arg259Ser
|
|
XM_011517569.1:c.870G>T
(CPA6)
|
XP_011515871.1:p.Arg290Ser
|
|
XM_011517570.1:c.333G>T
(CPA6)
|
XP_011515872.1:p.Arg111Ser
|
|
NR_136224.1:n.694-7136C>A
(ARFGEF1-DT)
|
|
|
XM_011517570.2:c.333G>T
(CPA6)
|
XP_011515872.1:p.Arg111Ser
|
|
XM_017013646.1:c.333G>T
(CPA6)
|
XP_016869135.1:p.Arg111Ser
|
|
XR_001745565.1:n.1585G>T
(CPA6)
|
|
|
NM_020361.5:c.777G>T
(CPA6)
MANE Select
|
NP_065094.3:p.Arg259Ser
|
|