ENST00000264414.9:c.1335T>G
MANE Select
|
ENSP00000264414.4:p.Ser445Arg
|
|
ENST00000264414.8:c.1335T>G
|
ENSP00000264414.4:p.Ser445Arg
|
|
ENST00000344951.8:c.1137T>G
|
ENSP00000343601.4:p.Ser379Arg
|
|
ENST00000409096.5:c.1263T>G
|
ENSP00000387200.1:p.Ser421Arg
|
|
ENST00000409777.5:c.1263T>G
|
ENSP00000386525.1:p.Ser421Arg
|
|
ENST00000481135.1:n.631T>G
|
|
|
ENST00000617432.4:c.59T>G
|
ENSP00000477851.1:p.Val20Gly
|
|
NM_001257197.1:c.1137T>G
|
NP_001244126.1:p.Ser379Arg
|
|
NM_001257198.1:c.1353T>G
|
NP_001244127.1:p.Ser451Arg
|
|
NM_003590.4:c.1335T>G
|
NP_003581.1:p.Ser445Arg
|
|
XM_006712800.2:c.1302T>G
|
XP_006712863.2:p.Ser434Arg
|
|
XM_011511994.1:c.1188T>G
|
XP_011510296.1:p.Ser396Arg
|
|
XM_011511995.1:c.1293T>G
|
XP_011510297.1:p.Ser431Arg
|
|
XM_011511996.1:c.1143T>G
|
XP_011510298.1:p.Ser381Arg
|
|
XM_011511997.1:c.1035T>G
|
XP_011510299.1:p.Ser345Arg
|
|
XM_011511994.3:c.1188T>G
|
XP_011510296.1:p.Ser396Arg
|
|
XM_011511996.2:c.1143T>G
|
XP_011510298.1:p.Ser381Arg
|
|
NM_003590.5:c.1335T>G
MANE Select
|
NP_003581.1:p.Ser445Arg
|
|
NM_001257198.2:c.1353T>G
|
NP_001244127.1:p.Ser451Arg
|
|
NM_001257197.2:c.1137T>G
|
NP_001244126.1:p.Ser379Arg
|
|