ENST00000209873.9:c.1568C>G
MANE Select
|
ENSP00000209873.4:p.Pro523Arg
|
|
ENST00000546562.6:n.2632C>G
|
|
|
ENST00000547238.6:n.2204C>G
|
|
|
ENST00000547520.6:n.1684C>G
|
|
|
ENST00000547757.2:c.*486C>G
|
ENSP00000448020.2:n.*486C>G
|
|
ENST00000548931.6:c.1003C>G
|
ENSP00000457518.1:p.Gln335Glu
|
|
ENST00000549450.6:n.1502C>G
|
|
|
ENST00000672797.1:n.2057C>G
|
|
|
ENST00000209873.8:c.1568C>G
|
ENSP00000209873.4:p.Pro523Arg
|
|
ENST00000394384.7:c.1469C>G
|
ENSP00000377908.3:p.Pro490Arg
|
|
ENST00000548931.5:c.1003C>G
|
ENSP00000457518.1:p.Gln335Glu
|
|
ENST00000550286.5:c.1196C>G
|
ENSP00000446885.1:p.Pro399Arg
|
|
ENST00000552876.5:n.1911C>G
|
|
|
NM_001173466.1:c.1469C>G
|
NP_001166937.1:p.Pro490Arg
|
|
NM_015665.5:c.1568C>G
|
NP_056480.1:p.Pro523Arg
|
|
XM_006719617.2:c.1583C>G
|
XP_006719680.1:p.Pro528Arg
|
|
XM_011538777.1:c.1625C>G
|
XP_011537079.1:p.Pro542Arg
|
|
XM_011538778.1:c.1610C>G
|
XP_011537080.1:p.Pro537Arg
|
|
XM_011538779.1:c.1526C>G
|
XP_011537081.1:p.Pro509Arg
|
|
XM_011538780.1:c.1511C>G
|
XP_011537082.1:p.Pro504Arg
|
|
XM_011538781.1:c.959C>G
|
XP_011537083.1:p.Pro320Arg
|
|
XM_011538778.2:c.1610C>G
|
XP_011537080.1:p.Pro537Arg
|
|
XM_011538780.2:c.1511C>G
|
XP_011537082.1:p.Pro504Arg
|
|
XR_001748875.2:n.1625C>G
|
|
|
NM_015665.6:c.1568C>G
MANE Select
|
NP_056480.1:p.Pro523Arg
|
|
NM_001173466.2:c.1469C>G
|
NP_001166937.1:p.Pro490Arg
|
|