ENST00000209873.9:c.1602A>T
MANE Select
|
ENSP00000209873.4:p.Pro534=
|
|
ENST00000546562.6:n.2666A>T
|
|
|
ENST00000547238.6:n.2238A>T
|
|
|
ENST00000547757.2:c.*520A>T
|
ENSP00000448020.2:n.*520A>T
|
|
ENST00000548931.6:c.1037A>T
|
ENSP00000457518.1:p.His346Leu
|
|
ENST00000549450.6:n.1536A>T
|
|
|
ENST00000672797.1:n.2091A>T
|
|
|
ENST00000209873.8:c.1602A>T
|
ENSP00000209873.4:p.Pro534=
|
|
ENST00000394384.7:c.1503A>T
|
ENSP00000377908.3:p.Pro501=
|
|
ENST00000548931.5:c.1037A>T
|
ENSP00000457518.1:p.His346Leu
|
|
ENST00000550286.5:c.1230A>T
|
ENSP00000446885.1:p.Pro410=
|
|
ENST00000552876.5:n.1945A>T
|
|
|
NM_001173466.1:c.1503A>T
|
NP_001166937.1:p.Pro501=
|
|
NM_015665.5:c.1602A>T
|
NP_056480.1:p.Pro534=
|
|
XM_006719617.2:c.1617A>T
|
XP_006719680.1:p.Pro539=
|
|
XM_011538777.1:c.1659A>T
|
XP_011537079.1:p.Pro553=
|
|
XM_011538778.1:c.1644A>T
|
XP_011537080.1:p.Pro548=
|
|
XM_011538779.1:c.1560A>T
|
XP_011537081.1:p.Pro520=
|
|
XM_011538780.1:c.1545A>T
|
XP_011537082.1:p.Pro515=
|
|
XM_011538781.1:c.993A>T
|
XP_011537083.1:p.Pro331=
|
|
XM_011538778.2:c.1644A>T
|
XP_011537080.1:p.Pro548=
|
|
XM_011538780.2:c.1545A>T
|
XP_011537082.1:p.Pro515=
|
|
XR_001748875.2:n.1659A>T
|
|
|
NM_015665.6:c.1602A>T
MANE Select
|
NP_056480.1:p.Pro534=
|
|
NM_001173466.2:c.1503A>T
|
NP_001166937.1:p.Pro501=
|
|