ENST00000209873.9:c.1515T>G
MANE Select
|
ENSP00000209873.4:p.Pro505=
|
|
ENST00000546562.6:n.2579T>G
|
|
|
ENST00000547238.6:n.2151T>G
|
|
|
ENST00000547520.6:n.1631T>G
|
|
|
ENST00000547757.2:c.*433T>G
|
ENSP00000448020.2:n.*433T>G
|
|
ENST00000548931.6:c.950T>G
|
ENSP00000457518.1:p.Leu317Arg
|
|
ENST00000549450.6:n.1449T>G
|
|
|
ENST00000672797.1:n.2004T>G
|
|
|
ENST00000209873.8:c.1515T>G
|
ENSP00000209873.4:p.Pro505=
|
|
ENST00000394384.7:c.1416T>G
|
ENSP00000377908.3:p.Pro472=
|
|
ENST00000548931.5:c.950T>G
|
ENSP00000457518.1:p.Leu317Arg
|
|
ENST00000550286.5:c.1143T>G
|
ENSP00000446885.1:p.Pro381=
|
|
ENST00000552876.5:n.1858T>G
|
|
|
NM_001173466.1:c.1416T>G
|
NP_001166937.1:p.Pro472=
|
|
NM_015665.5:c.1515T>G
|
NP_056480.1:p.Pro505=
|
|
XM_006719617.2:c.1530T>G
|
XP_006719680.1:p.Pro510=
|
|
XM_011538777.1:c.1572T>G
|
XP_011537079.1:p.Pro524=
|
|
XM_011538778.1:c.1557T>G
|
XP_011537080.1:p.Pro519=
|
|
XM_011538779.1:c.1473T>G
|
XP_011537081.1:p.Pro491=
|
|
XM_011538780.1:c.1458T>G
|
XP_011537082.1:p.Pro486=
|
|
XM_011538781.1:c.906T>G
|
XP_011537083.1:p.Pro302=
|
|
XM_011538778.2:c.1557T>G
|
XP_011537080.1:p.Pro519=
|
|
XM_011538780.2:c.1458T>G
|
XP_011537082.1:p.Pro486=
|
|
XR_001748875.2:n.1572T>G
|
|
|
NM_015665.6:c.1515T>G
MANE Select
|
NP_056480.1:p.Pro505=
|
|
NM_001173466.2:c.1416T>G
|
NP_001166937.1:p.Pro472=
|
|