ENST00000209873.9:c.1625C>G
MANE Select
|
ENSP00000209873.4:p.Pro542Arg
|
|
ENST00000546562.6:n.2689C>G
|
|
|
ENST00000547757.2:c.*543C>G
|
ENSP00000448020.2:n.*543C>G
|
|
ENST00000548931.6:c.1060C>G
|
ENSP00000457518.1:p.His354Asp
|
|
ENST00000549450.6:n.1559C>G
|
|
|
ENST00000209873.8:c.1625C>G
|
ENSP00000209873.4:p.Pro542Arg
|
|
ENST00000394384.7:c.1526C>G
|
ENSP00000377908.3:p.Pro509Arg
|
|
ENST00000548931.5:c.1060C>G
|
ENSP00000457518.1:p.His354Asp
|
|
ENST00000550286.5:c.1253C>G
|
ENSP00000446885.1:p.Pro418Arg
|
|
ENST00000552876.5:n.1968C>G
|
|
|
NM_001173466.1:c.1526C>G
|
NP_001166937.1:p.Pro509Arg
|
|
NM_015665.5:c.1625C>G
|
NP_056480.1:p.Pro542Arg
|
|
XM_006719617.2:c.1640C>G
|
XP_006719680.1:p.Pro547Arg
|
|
XM_011538777.1:c.1682C>G
|
XP_011537079.1:p.Pro561Arg
|
|
XM_011538778.1:c.1667C>G
|
XP_011537080.1:p.Pro556Arg
|
|
XM_011538779.1:c.1583C>G
|
XP_011537081.1:p.Pro528Arg
|
|
XM_011538780.1:c.1568C>G
|
XP_011537082.1:p.Pro523Arg
|
|
XM_011538781.1:c.1016C>G
|
XP_011537083.1:p.Pro339Arg
|
|
XM_011538778.2:c.1667C>G
|
XP_011537080.1:p.Pro556Arg
|
|
XM_011538780.2:c.1568C>G
|
XP_011537082.1:p.Pro523Arg
|
|
XR_001748875.2:n.1682C>G
|
|
|
NM_015665.6:c.1625C>G
MANE Select
|
NP_056480.1:p.Pro542Arg
|
|
NM_001173466.2:c.1526C>G
|
NP_001166937.1:p.Pro509Arg
|
|