ENST00000209873.9:c.1626A>T
MANE Select
|
ENSP00000209873.4:p.Pro542=
|
|
ENST00000546562.6:n.2690A>T
|
|
|
ENST00000547757.2:c.*544A>T
|
ENSP00000448020.2:n.*544A>T
|
|
ENST00000548931.6:c.1061A>T
|
ENSP00000457518.1:p.His354Leu
|
|
ENST00000549450.6:n.1560A>T
|
|
|
ENST00000209873.8:c.1626A>T
|
ENSP00000209873.4:p.Pro542=
|
|
ENST00000394384.7:c.1527A>T
|
ENSP00000377908.3:p.Pro509=
|
|
ENST00000548931.5:c.1061A>T
|
ENSP00000457518.1:p.His354Leu
|
|
ENST00000550286.5:c.1254A>T
|
ENSP00000446885.1:p.Pro418=
|
|
ENST00000552876.5:n.1969A>T
|
|
|
NM_001173466.1:c.1527A>T
|
NP_001166937.1:p.Pro509=
|
|
NM_015665.5:c.1626A>T
|
NP_056480.1:p.Pro542=
|
|
XM_006719617.2:c.1641A>T
|
XP_006719680.1:p.Pro547=
|
|
XM_011538777.1:c.1683A>T
|
XP_011537079.1:p.Pro561=
|
|
XM_011538778.1:c.1668A>T
|
XP_011537080.1:p.Pro556=
|
|
XM_011538779.1:c.1584A>T
|
XP_011537081.1:p.Pro528=
|
|
XM_011538780.1:c.1569A>T
|
XP_011537082.1:p.Pro523=
|
|
XM_011538781.1:c.1017A>T
|
XP_011537083.1:p.Pro339=
|
|
XM_011538778.2:c.1668A>T
|
XP_011537080.1:p.Pro556=
|
|
XM_011538780.2:c.1569A>T
|
XP_011537082.1:p.Pro523=
|
|
XR_001748875.2:n.1683A>T
|
|
|
NM_015665.6:c.1626A>T
MANE Select
|
NP_056480.1:p.Pro542=
|
|
NM_001173466.2:c.1527A>T
|
NP_001166937.1:p.Pro509=
|
|