ENST00000297770.10:c.803T=
(CPA6)
MANE Select
|
ENSP00000297770.4:p.Val268=
|
|
ENST00000638254.1:c.*399T=
(CPA6)
|
ENSP00000491129.1:n.*399T=
|
|
ENST00000297770.8:c.803T=
(CPA6)
|
ENSP00000297770.4:p.Val268=
|
|
ENST00000479862.6:c.*399T=
(CPA6)
|
ENSP00000419016.2:n.*399T=
|
|
ENST00000518549.1:c.803T=
(CPA6)
|
ENSP00000431112.1:p.Val268=
|
|
NM_020361.4:c.803T=
(CPA6)
|
NP_065094.3:p.Val268=
|
|
XM_011517569.1:c.896T=
(CPA6)
|
XP_011515871.1:p.Val299=
|
|
XM_011517570.1:c.359T=
(CPA6)
|
XP_011515872.1:p.Val120=
|
|
NR_136224.1:n.694-7162A=
(ARFGEF1-DT)
|
|
|
XM_011517570.2:c.359T=
(CPA6)
|
XP_011515872.1:p.Val120=
|
|
XM_017013646.1:c.359T=
(CPA6)
|
XP_016869135.1:p.Val120=
|
|
XR_001745565.1:n.1611T=
(CPA6)
|
|
|
NM_020361.5:c.803T=
(CPA6)
MANE Select
|
NP_065094.3:p.Val268=
|
|