ENST00000209873.9:c.1488A>G
MANE Select
|
ENSP00000209873.4:p.Pro496=
|
|
ENST00000546562.6:n.2552A>G
|
|
|
ENST00000547238.6:n.2124A>G
|
|
|
ENST00000547520.6:n.1604A>G
|
|
|
ENST00000547757.2:c.*406A>G
|
ENSP00000448020.2:n.*406A>G
|
|
ENST00000548931.6:c.923A>G
|
ENSP00000457518.1:p.Gln308Arg
|
|
ENST00000549450.6:n.1422A>G
|
|
|
ENST00000552161.6:n.2566A>G
|
|
|
ENST00000672797.1:n.1977A>G
|
|
|
ENST00000209873.8:c.1488A>G
|
ENSP00000209873.4:p.Pro496=
|
|
ENST00000394384.7:c.1389A>G
|
ENSP00000377908.3:p.Pro463=
|
|
ENST00000548931.5:c.923A>G
|
ENSP00000457518.1:p.Gln308Arg
|
|
ENST00000550286.5:c.1116A>G
|
ENSP00000446885.1:p.Pro372=
|
|
ENST00000552876.5:n.1831A>G
|
|
|
NM_001173466.1:c.1389A>G
|
NP_001166937.1:p.Pro463=
|
|
NM_015665.5:c.1488A>G
|
NP_056480.1:p.Pro496=
|
|
XM_006719617.2:c.1503A>G
|
XP_006719680.1:p.Pro501=
|
|
XM_011538777.1:c.1545A>G
|
XP_011537079.1:p.Pro515=
|
|
XM_011538778.1:c.1530A>G
|
XP_011537080.1:p.Pro510=
|
|
XM_011538779.1:c.1446A>G
|
XP_011537081.1:p.Pro482=
|
|
XM_011538780.1:c.1431A>G
|
XP_011537082.1:p.Pro477=
|
|
XM_011538781.1:c.879A>G
|
XP_011537083.1:p.Pro293=
|
|
XM_011538778.2:c.1530A>G
|
XP_011537080.1:p.Pro510=
|
|
XM_011538780.2:c.1431A>G
|
XP_011537082.1:p.Pro477=
|
|
XR_001748875.2:n.1545A>G
|
|
|
NM_015665.6:c.1488A>G
MANE Select
|
NP_056480.1:p.Pro496=
|
|
NM_001173466.2:c.1389A>G
|
NP_001166937.1:p.Pro463=
|
|