ENST00000209873.9:c.1624C>T
MANE Select
|
ENSP00000209873.4:p.Pro542Ser
|
|
ENST00000546562.6:n.2688C>T
|
|
|
ENST00000547757.2:c.*542C>T
|
ENSP00000448020.2:n.*542C>T
|
|
ENST00000548931.6:c.1059C>T
|
ENSP00000457518.1:p.Pro353=
|
|
ENST00000549450.6:n.1558C>T
|
|
|
ENST00000209873.8:c.1624C>T
|
ENSP00000209873.4:p.Pro542Ser
|
|
ENST00000394384.7:c.1525C>T
|
ENSP00000377908.3:p.Pro509Ser
|
|
ENST00000548931.5:c.1059C>T
|
ENSP00000457518.1:p.Pro353=
|
|
ENST00000550286.5:c.1252C>T
|
ENSP00000446885.1:p.Pro418Ser
|
|
ENST00000552876.5:n.1967C>T
|
|
|
NM_001173466.1:c.1525C>T
|
NP_001166937.1:p.Pro509Ser
|
|
NM_015665.5:c.1624C>T
|
NP_056480.1:p.Pro542Ser
|
|
XM_006719617.2:c.1639C>T
|
XP_006719680.1:p.Pro547Ser
|
|
XM_011538777.1:c.1681C>T
|
XP_011537079.1:p.Pro561Ser
|
|
XM_011538778.1:c.1666C>T
|
XP_011537080.1:p.Pro556Ser
|
|
XM_011538779.1:c.1582C>T
|
XP_011537081.1:p.Pro528Ser
|
|
XM_011538780.1:c.1567C>T
|
XP_011537082.1:p.Pro523Ser
|
|
XM_011538781.1:c.1015C>T
|
XP_011537083.1:p.Pro339Ser
|
|
XM_011538778.2:c.1666C>T
|
XP_011537080.1:p.Pro556Ser
|
|
XM_011538780.2:c.1567C>T
|
XP_011537082.1:p.Pro523Ser
|
|
XR_001748875.2:n.1681C>T
|
|
|
NM_015665.6:c.1624C>T
MANE Select
|
NP_056480.1:p.Pro542Ser
|
|
NM_001173466.2:c.1525C>T
|
NP_001166937.1:p.Pro509Ser
|
|