ENST00000209873.9:c.1077A>T
MANE Select
|
ENSP00000209873.4:p.Pro359=
|
|
ENST00000546562.6:n.2141A>T
|
|
|
ENST00000547238.6:n.1713A>T
|
|
|
ENST00000547520.6:n.1071A>T
|
|
|
ENST00000547757.2:c.126A>T
|
ENSP00000448020.2:p.Pro42=
|
|
ENST00000548880.2:n.1527A>T
|
|
|
ENST00000548931.6:c.597A>T
|
ENSP00000457518.1:p.Pro199=
|
|
ENST00000549450.6:n.1011A>T
|
|
|
ENST00000552161.6:n.2033A>T
|
|
|
ENST00000672797.1:n.1566A>T
|
|
|
ENST00000672900.1:n.2019A>T
|
|
|
ENST00000209873.8:c.1077A>T
|
ENSP00000209873.4:p.Pro359=
|
|
ENST00000394384.7:c.978A>T
|
ENSP00000377908.3:p.Pro326=
|
|
ENST00000548931.5:c.597A>T
|
ENSP00000457518.1:p.Pro199=
|
|
ENST00000550033.5:n.332A>T
|
|
|
ENST00000550286.5:c.705A>T
|
ENSP00000446885.1:p.Pro235=
|
|
ENST00000552876.5:n.1420A>T
|
|
|
NM_001173466.1:c.978A>T
|
NP_001166937.1:p.Pro326=
|
|
NM_015665.5:c.1077A>T
|
NP_056480.1:p.Pro359=
|
|
XM_006719617.2:c.1092A>T
|
XP_006719680.1:p.Pro364=
|
|
XM_011538777.1:c.1092A>T
|
XP_011537079.1:p.Pro364=
|
|
XM_011538778.1:c.1077A>T
|
XP_011537080.1:p.Pro359=
|
|
XM_011538779.1:c.993A>T
|
XP_011537081.1:p.Pro331=
|
|
XM_011538780.1:c.978A>T
|
XP_011537082.1:p.Pro326=
|
|
XM_011538781.1:c.426A>T
|
XP_011537083.1:p.Pro142=
|
|
XM_011538778.2:c.1077A>T
|
XP_011537080.1:p.Pro359=
|
|
XM_011538780.2:c.978A>T
|
XP_011537082.1:p.Pro326=
|
|
XR_001748875.2:n.1134A>T
|
|
|
NM_015665.6:c.1077A>T
MANE Select
|
NP_056480.1:p.Pro359=
|
|
NM_001173466.2:c.978A>T
|
NP_001166937.1:p.Pro326=
|
|