ENST00000255078.8:c.1408C>G
MANE Select
|
ENSP00000255078.4:p.His470Asp
|
|
ENST00000536803.2:n.319C>G
|
|
|
ENST00000674955.1:c.*125C>G
|
ENSP00000502463.1:n.*125C>G
|
|
ENST00000675118.1:c.896C>G
|
|
|
ENST00000675205.1:n.173C>G
|
|
|
ENST00000675310.1:n.545C>G
|
|
|
ENST00000675615.1:c.1408C>G
|
ENSP00000502413.1:p.His470Asp
|
|
ENST00000675648.1:n.783C>G
|
|
|
ENST00000675997.1:n.113-993C>G
|
|
|
ENST00000676149.1:n.482C>G
|
|
|
ENST00000676173.1:n.2153C>G
|
|
|
ENST00000676228.1:c.*731C>G
|
ENSP00000502375.1:n.*731C>G
|
|
ENST00000255078.7:c.1408C>G
|
ENSP00000255078.3:p.His470Asp
|
|
ENST00000537458.5:n.525C>G
|
|
|
ENST00000539064.5:n.1167C>G
|
|
|
ENST00000543739.5:n.525C>G
|
|
|
NM_002180.2:c.1408C>G , LRG_250t1:c.1408C>G
|
NP_002171.2:p.His470Asp
|
|
XM_005273974.2:c.397C>G
|
XP_005274031.1:p.His133Asp
|
|
XM_005273975.2:c.280C>G
|
XP_005274032.1:p.His94Asp
|
|
XM_011544994.1:c.175C>G
|
XP_011543296.1:p.His59Asp
|
|
XR_949903.1:n.1510C>G
|
|
|
XM_005273975.3:c.280C>G
|
XP_005274032.1:p.His94Asp
|
|
XM_017017669.2:c.397C>G
|
XP_016873158.1:p.His133Asp
|
|
XM_017017670.2:c.397C>G
|
XP_016873159.1:p.His133Asp
|
|
XM_017017671.2:c.1408C>G
|
XP_016873160.1:p.His470Asp
|
|
XR_949903.3:n.1506C>G
|
|
|
NM_002180.3:c.1408C>G
MANE Select
|
NP_002171.2:p.His470Asp
|
|