ENST00000209873.9:c.1550T>C
MANE Select
|
ENSP00000209873.4:p.Leu517Pro
|
|
ENST00000546562.6:n.2614T>C
|
|
|
ENST00000547238.6:n.2186T>C
|
|
|
ENST00000547520.6:n.1666T>C
|
|
|
ENST00000547757.2:c.*468T>C
|
ENSP00000448020.2:n.*468T>C
|
|
ENST00000548931.6:c.985T>C
|
ENSP00000457518.1:p.Ser329Pro
|
|
ENST00000549450.6:n.1484T>C
|
|
|
ENST00000672797.1:n.2039T>C
|
|
|
ENST00000209873.8:c.1550T>C
|
ENSP00000209873.4:p.Leu517Pro
|
|
ENST00000394384.7:c.1451T>C
|
ENSP00000377908.3:p.Leu484Pro
|
|
ENST00000548931.5:c.985T>C
|
ENSP00000457518.1:p.Ser329Pro
|
|
ENST00000550286.5:c.1178T>C
|
ENSP00000446885.1:p.Leu393Pro
|
|
ENST00000552876.5:n.1893T>C
|
|
|
NM_001173466.1:c.1451T>C
|
NP_001166937.1:p.Leu484Pro
|
|
NM_015665.5:c.1550T>C
|
NP_056480.1:p.Leu517Pro
|
|
XM_006719617.2:c.1565T>C
|
XP_006719680.1:p.Leu522Pro
|
|
XM_011538777.1:c.1607T>C
|
XP_011537079.1:p.Leu536Pro
|
|
XM_011538778.1:c.1592T>C
|
XP_011537080.1:p.Leu531Pro
|
|
XM_011538779.1:c.1508T>C
|
XP_011537081.1:p.Leu503Pro
|
|
XM_011538780.1:c.1493T>C
|
XP_011537082.1:p.Leu498Pro
|
|
XM_011538781.1:c.941T>C
|
XP_011537083.1:p.Leu314Pro
|
|
XM_011538778.2:c.1592T>C
|
XP_011537080.1:p.Leu531Pro
|
|
XM_011538780.2:c.1493T>C
|
XP_011537082.1:p.Leu498Pro
|
|
XR_001748875.2:n.1607T>C
|
|
|
NM_015665.6:c.1550T>C
MANE Select
|
NP_056480.1:p.Leu517Pro
|
|
NM_001173466.2:c.1451T>C
|
NP_001166937.1:p.Leu484Pro
|
|