ENST00000209873.9:c.1581T>G
MANE Select
|
ENSP00000209873.4:p.Pro527=
|
|
ENST00000546562.6:n.2645T>G
|
|
|
ENST00000547238.6:n.2217T>G
|
|
|
ENST00000547520.6:n.1697T>G
|
|
|
ENST00000547757.2:c.*499T>G
|
ENSP00000448020.2:n.*499T>G
|
|
ENST00000548931.6:c.1016T>G
|
ENSP00000457518.1:p.Leu339Arg
|
|
ENST00000549450.6:n.1515T>G
|
|
|
ENST00000672797.1:n.2070T>G
|
|
|
ENST00000209873.8:c.1581T>G
|
ENSP00000209873.4:p.Pro527=
|
|
ENST00000394384.7:c.1482T>G
|
ENSP00000377908.3:p.Pro494=
|
|
ENST00000548931.5:c.1016T>G
|
ENSP00000457518.1:p.Leu339Arg
|
|
ENST00000550286.5:c.1209T>G
|
ENSP00000446885.1:p.Pro403=
|
|
ENST00000552876.5:n.1924T>G
|
|
|
NM_001173466.1:c.1482T>G
|
NP_001166937.1:p.Pro494=
|
|
NM_015665.5:c.1581T>G
|
NP_056480.1:p.Pro527=
|
|
XM_006719617.2:c.1596T>G
|
XP_006719680.1:p.Pro532=
|
|
XM_011538777.1:c.1638T>G
|
XP_011537079.1:p.Pro546=
|
|
XM_011538778.1:c.1623T>G
|
XP_011537080.1:p.Pro541=
|
|
XM_011538779.1:c.1539T>G
|
XP_011537081.1:p.Pro513=
|
|
XM_011538780.1:c.1524T>G
|
XP_011537082.1:p.Pro508=
|
|
XM_011538781.1:c.972T>G
|
XP_011537083.1:p.Pro324=
|
|
XM_011538778.2:c.1623T>G
|
XP_011537080.1:p.Pro541=
|
|
XM_011538780.2:c.1524T>G
|
XP_011537082.1:p.Pro508=
|
|
XR_001748875.2:n.1638T>G
|
|
|
NM_015665.6:c.1581T>G
MANE Select
|
NP_056480.1:p.Pro527=
|
|
NM_001173466.2:c.1482T>G
|
NP_001166937.1:p.Pro494=
|
|