ENST00000392446.10:c.763G>C
MANE Select
|
ENSP00000376241.4:p.Gly255Arg
|
|
ENST00000302345.6:c.763G>C
|
ENSP00000307674.2:p.Gly255Arg
|
|
ENST00000392446.9:c.763G>C
|
ENSP00000376241.4:p.Gly255Arg
|
|
ENST00000588096.1:n.160G>C
|
|
|
ENST00000591773.5:c.763G>C
|
ENSP00000467437.1:p.Gly255Arg
|
|
ENST00000592228.1:c.647+1886G>C
|
ENSP00000466743.1:n.647+1886G>C
|
|
ENST00000620915.4:c.763G>C
|
ENSP00000477798.1:p.Gly255Arg
|
|
NM_001159772.1:c.763G>C
|
NP_001153244.1:p.Gly255Arg
|
|
NM_001159773.1:c.763G>C
|
NP_001153245.1:p.Gly255Arg
|
|
NM_138793.3:c.763G>C
|
NP_620148.1:p.Gly255Arg
|
|
XM_005257020.1:c.763G>C
|
XP_005257077.1:p.Gly255Arg
|
|
XM_005257021.1:c.763G>C
|
XP_005257078.1:p.Gly255Arg
|
|
XM_005257022.1:c.763G>C
|
XP_005257079.1:p.Gly255Arg
|
|
XM_006721683.1:c.763G>C
|
XP_006721746.1:p.Gly255Arg
|
|
XM_011524291.1:c.763G>C
|
XP_011522593.1:p.Gly255Arg
|
|
XM_011524292.1:c.763G>C
|
XP_011522594.1:p.Gly255Arg
|
|
XM_011524293.1:c.763G>C
|
XP_011522595.1:p.Gly255Arg
|
|
XM_011524294.1:c.763G>C
|
XP_011522596.1:p.Gly255Arg
|
|
XM_011524295.1:c.763G>C
|
XP_011522597.1:p.Gly255Arg
|
|
XM_011524294.2:c.763G>C
|
XP_011522596.1:p.Gly255Arg
|
|
XM_011524295.2:c.763G>C
|
XP_011522597.1:p.Gly255Arg
|
|
XM_024450564.1:c.763G>C
|
XP_024306332.1:p.Gly255Arg
|
|
XR_001752424.2:n.1207G>C
|
|
|
NM_001159773.2:c.763G>C
MANE Select
|
NP_001153245.1:p.Gly255Arg
|
|
NM_001159772.2:c.763G>C
|
NP_001153244.1:p.Gly255Arg
|
|
NM_138793.4:c.763G>C
|
NP_620148.1:p.Gly255Arg
|
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