ENST00000209873.9:c.1075C>T
MANE Select
|
ENSP00000209873.4:p.Pro359Ser
|
|
ENST00000546562.6:n.2139C>T
|
|
|
ENST00000547238.6:n.1711C>T
|
|
|
ENST00000547520.6:n.1069C>T
|
|
|
ENST00000547757.2:c.124C>T
|
ENSP00000448020.2:p.Pro42Ser
|
|
ENST00000548880.2:n.1525C>T
|
|
|
ENST00000548931.6:c.595C>T
|
ENSP00000457518.1:p.Pro199Ser
|
|
ENST00000549450.6:n.1009C>T
|
|
|
ENST00000552161.6:n.2031C>T
|
|
|
ENST00000672797.1:n.1564C>T
|
|
|
ENST00000672900.1:n.2017C>T
|
|
|
ENST00000209873.8:c.1075C>T
|
ENSP00000209873.4:p.Pro359Ser
|
|
ENST00000394384.7:c.976C>T
|
ENSP00000377908.3:p.Pro326Ser
|
|
ENST00000548931.5:c.595C>T
|
ENSP00000457518.1:p.Pro199Ser
|
|
ENST00000550033.5:n.330C>T
|
|
|
ENST00000550286.5:c.703C>T
|
ENSP00000446885.1:p.Pro235Ser
|
|
ENST00000552876.5:n.1418C>T
|
|
|
NM_001173466.1:c.976C>T
|
NP_001166937.1:p.Pro326Ser
|
|
NM_015665.5:c.1075C>T
|
NP_056480.1:p.Pro359Ser
|
|
XM_006719617.2:c.1090C>T
|
XP_006719680.1:p.Pro364Ser
|
|
XM_011538777.1:c.1090C>T
|
XP_011537079.1:p.Pro364Ser
|
|
XM_011538778.1:c.1075C>T
|
XP_011537080.1:p.Pro359Ser
|
|
XM_011538779.1:c.991C>T
|
XP_011537081.1:p.Pro331Ser
|
|
XM_011538780.1:c.976C>T
|
XP_011537082.1:p.Pro326Ser
|
|
XM_011538781.1:c.424C>T
|
XP_011537083.1:p.Pro142Ser
|
|
XM_011538778.2:c.1075C>T
|
XP_011537080.1:p.Pro359Ser
|
|
XM_011538780.2:c.976C>T
|
XP_011537082.1:p.Pro326Ser
|
|
XR_001748875.2:n.1132C>T
|
|
|
NM_015665.6:c.1075C>T
MANE Select
|
NP_056480.1:p.Pro359Ser
|
|
NM_001173466.2:c.976C>T
|
NP_001166937.1:p.Pro326Ser
|
|