ENST00000209873.9:c.1512C>G
MANE Select
|
ENSP00000209873.4:p.Pro504=
|
|
ENST00000546562.6:n.2576C>G
|
|
|
ENST00000547238.6:n.2148C>G
|
|
|
ENST00000547520.6:n.1628C>G
|
|
|
ENST00000547757.2:c.*430C>G
|
ENSP00000448020.2:n.*430C>G
|
|
ENST00000548931.6:c.947C>G
|
ENSP00000457518.1:p.Pro316Arg
|
|
ENST00000549450.6:n.1446C>G
|
|
|
ENST00000672797.1:n.2001C>G
|
|
|
ENST00000209873.8:c.1512C>G
|
ENSP00000209873.4:p.Pro504=
|
|
ENST00000394384.7:c.1413C>G
|
ENSP00000377908.3:p.Pro471=
|
|
ENST00000548931.5:c.947C>G
|
ENSP00000457518.1:p.Pro316Arg
|
|
ENST00000550286.5:c.1140C>G
|
ENSP00000446885.1:p.Pro380=
|
|
ENST00000552876.5:n.1855C>G
|
|
|
NM_001173466.1:c.1413C>G
|
NP_001166937.1:p.Pro471=
|
|
NM_015665.5:c.1512C>G
|
NP_056480.1:p.Pro504=
|
|
XM_006719617.2:c.1527C>G
|
XP_006719680.1:p.Pro509=
|
|
XM_011538777.1:c.1569C>G
|
XP_011537079.1:p.Pro523=
|
|
XM_011538778.1:c.1554C>G
|
XP_011537080.1:p.Pro518=
|
|
XM_011538779.1:c.1470C>G
|
XP_011537081.1:p.Pro490=
|
|
XM_011538780.1:c.1455C>G
|
XP_011537082.1:p.Pro485=
|
|
XM_011538781.1:c.903C>G
|
XP_011537083.1:p.Pro301=
|
|
XM_011538778.2:c.1554C>G
|
XP_011537080.1:p.Pro518=
|
|
XM_011538780.2:c.1455C>G
|
XP_011537082.1:p.Pro485=
|
|
XR_001748875.2:n.1569C>G
|
|
|
NM_015665.6:c.1512C>G
MANE Select
|
NP_056480.1:p.Pro504=
|
|
NM_001173466.2:c.1413C>G
|
NP_001166937.1:p.Pro471=
|
|