|
ENST00000324464.8:c.691G=
MANE Select
|
ENSP00000315118.3:p.Gly231=
|
|
|
ENST00000593724.2:n.393-119G=
|
|
|
|
ENST00000594490.6:c.613G=
|
ENSP00000471310.2:p.Gly205=
|
|
|
ENST00000594720.6:c.691G=
|
ENSP00000470876.2:p.Gly231=
|
|
|
ENST00000596455.6:n.983G=
|
|
|
|
ENST00000601967.6:c.691G=
|
ENSP00000470916.2:p.Gly231=
|
|
|
ENST00000676555.1:c.691G=
|
ENSP00000503387.1:p.Gly231=
|
|
|
ENST00000676578.1:c.*433G=
|
ENSP00000504076.1:n.*433G=
|
|
|
ENST00000676960.1:n.816G=
|
|
|
|
ENST00000676962.1:n.970G=
|
|
|
|
ENST00000677018.1:c.691G=
|
ENSP00000503480.1:p.Gly231=
|
|
|
ENST00000677039.1:n.746G=
|
|
|
|
ENST00000677399.1:n.1133G=
|
|
|
|
ENST00000677496.1:c.364G=
|
ENSP00000504773.1:p.Gly122=
|
|
|
ENST00000677517.1:c.364G=
|
ENSP00000503519.1:p.Gly122=
|
|
|
ENST00000677633.1:c.*114G=
|
ENSP00000503645.1:n.*114G=
|
|
|
ENST00000677800.1:c.*3795G=
|
ENSP00000503794.1:n.*3795G=
|
|
|
ENST00000678057.1:c.*255G=
|
ENSP00000503762.1:n.*255G=
|
|
|
ENST00000678119.1:n.885G=
|
|
|
|
ENST00000678166.1:n.861-119G=
|
|
|
|
ENST00000678312.1:n.1028G=
|
|
|
|
ENST00000678316.1:c.*114G=
|
ENSP00000504112.1:n.*114G=
|
|
|
ENST00000678371.1:n.1049G=
|
|
|
|
ENST00000678404.1:c.691G=
|
ENSP00000503944.1:p.Gly231=
|
|
|
ENST00000678419.1:c.691G=
|
ENSP00000504085.1:p.Gly231=
|
|
|
ENST00000678433.1:n.1051G=
|
|
|
|
ENST00000678467.1:c.691G=
|
ENSP00000504072.1:p.Gly231=
|
|
|
ENST00000678569.1:c.691G=
|
ENSP00000504261.1:p.Gly231=
|
|
|
ENST00000678961.1:n.874G=
|
|
|
|
ENST00000679002.1:n.870G=
|
|
|
|
ENST00000679012.1:c.247G=
|
ENSP00000504446.1:p.Gly83=
|
|
|
ENST00000679070.1:c.*114G=
|
ENSP00000503759.1:n.*114G=
|
|
|
ENST00000679130.1:c.691G=
|
ENSP00000504845.1:p.Gly231=
|
|
|
ENST00000679315.1:c.*521G=
|
ENSP00000503065.1:n.*521G=
|
|
|
ENST00000243583.10:c.568G=
|
ENSP00000243583.5:p.Gly190=
|
|
|
ENST00000324464.7:c.691G=
|
ENSP00000315118.3:p.Gly231=
|
|
|
ENST00000595254.5:c.364G=
|
ENSP00000470894.1:p.Gly122=
|
|
|
ENST00000596455.5:n.811G=
|
|
|
|
ENST00000599643.5:c.336-119G=
|
ENSP00000471192.1:n.336-119G=
|
|
|
ENST00000601304.5:c.*465G=
|
ENSP00000472519.1:n.*465G=
|
|
|
NM_001142555.2:c.568G=
|
NP_001136027.1:p.Gly190=
|
|
|
NM_024876.3:c.691G=
|
NP_079152.3:p.Gly231=
|
|
|
XM_005259270.3:c.853G=
|
XP_005259327.2:p.Gly285=
|
|
|
XM_005259271.3:c.691G=
|
XP_005259328.1:p.Gly231=
|
|
|
XM_005259272.3:c.691G=
|
XP_005259329.1:p.Gly231=
|
|
|
XM_005259273.3:c.691G=
|
XP_005259330.1:p.Gly231=
|
|
|
XM_006723392.2:c.691G=
|
XP_006723455.1:p.Gly231=
|
|
|
XM_006723393.2:c.691G=
|
XP_006723456.1:p.Gly231=
|
|
|
XM_011527334.1:c.691G=
|
XP_011525636.1:p.Gly231=
|
|
|
XM_011527335.1:c.577-119G=
|
XP_011525637.1:n.577-119G=
|
|
|
XM_011527336.1:c.721G=
|
XP_011525638.1:p.Gly241=
|
|
|
XM_011527337.1:c.691G=
|
XP_011525639.1:p.Gly231=
|
|
|
XM_011527338.1:c.691G=
|
XP_011525640.1:p.Gly231=
|
|
|
NM_024876.4:c.691G=
MANE Select
|
NP_079152.3:p.Gly231=
|
|
|
NM_001142555.3:c.568G=
|
NP_001136027.1:p.Gly190=
|
|
