ENST00000255078.8:c.1424T>G
MANE Select
|
ENSP00000255078.4:p.Leu475Arg
|
|
ENST00000674955.1:c.*141T>G
|
ENSP00000502463.1:n.*141T>G
|
|
ENST00000675118.1:c.912T>G
|
|
|
ENST00000675205.1:n.183+319T>G
|
|
|
ENST00000675615.1:c.1424T>G
|
ENSP00000502413.1:p.Leu475Arg
|
|
ENST00000675648.1:n.799T>G
|
|
|
ENST00000675997.1:n.113-664T>G
|
|
|
ENST00000676173.1:n.2169T>G
|
|
|
ENST00000676228.1:c.*747T>G
|
ENSP00000502375.1:n.*747T>G
|
|
ENST00000255078.7:c.1424T>G
|
ENSP00000255078.3:p.Leu475Arg
|
|
ENST00000537458.5:n.541T>G
|
|
|
ENST00000539064.5:n.1183T>G
|
|
|
ENST00000541229.5:n.119T>G
|
|
|
ENST00000543739.5:n.541T>G
|
|
|
NM_002180.2:c.1424T>G , LRG_250t1:c.1424T>G
|
NP_002171.2:p.Leu475Arg
|
|
XM_005273974.2:c.413T>G
|
XP_005274031.1:p.Leu138Arg
|
|
XM_005273975.2:c.296T>G
|
XP_005274032.1:p.Leu99Arg
|
|
XM_011544994.1:c.191T>G
|
XP_011543296.1:p.Leu64Arg
|
|
XR_949903.1:n.1526T>G
|
|
|
XM_005273975.3:c.296T>G
|
XP_005274032.1:p.Leu99Arg
|
|
XM_017017669.2:c.413T>G
|
XP_016873158.1:p.Leu138Arg
|
|
XM_017017670.2:c.413T>G
|
XP_016873159.1:p.Leu138Arg
|
|
XM_017017671.2:c.1424T>G
|
XP_016873160.1:p.Leu475Arg
|
|
XR_949903.3:n.1522T>G
|
|
|
NM_002180.3:c.1424T>G
MANE Select
|
NP_002171.2:p.Leu475Arg
|
|