ENST00000324464.8:c.987G>C
MANE Select
|
ENSP00000315118.3:p.Gly329=
|
|
ENST00000593724.2:n.2810G>C
|
|
|
ENST00000594490.6:c.909G>C
|
ENSP00000471310.2:p.Gly303=
|
|
ENST00000594720.6:c.987G>C
|
ENSP00000470876.2:p.Gly329=
|
|
ENST00000596455.6:n.1279G>C
|
|
|
ENST00000601967.6:c.987G>C
|
ENSP00000470916.2:p.Gly329=
|
|
ENST00000676555.1:c.987G>C
|
ENSP00000503387.1:p.Gly329=
|
|
ENST00000676578.1:c.*729G>C
|
ENSP00000504076.1:n.*729G>C
|
|
ENST00000676960.1:n.1112G>C
|
|
|
ENST00000676962.1:n.1266G>C
|
|
|
ENST00000677018.1:c.987G>C
|
ENSP00000503480.1:p.Gly329=
|
|
ENST00000677039.1:n.3190G>C
|
|
|
ENST00000677399.1:n.1429G>C
|
|
|
ENST00000677496.1:c.660G>C
|
ENSP00000504773.1:p.Gly220=
|
|
ENST00000677517.1:c.660G>C
|
ENSP00000503519.1:p.Gly220=
|
|
ENST00000677633.1:c.*410G>C
|
ENSP00000503645.1:n.*410G>C
|
|
ENST00000677800.1:c.*4091G>C
|
ENSP00000503794.1:n.*4091G>C
|
|
ENST00000678057.1:c.*551G>C
|
ENSP00000503762.1:n.*551G>C
|
|
ENST00000678119.1:n.1181G>C
|
|
|
ENST00000678166.1:n.1130G>C
|
|
|
ENST00000678312.1:n.1324G>C
|
|
|
ENST00000678316.1:c.*410G>C
|
ENSP00000504112.1:n.*410G>C
|
|
ENST00000678371.1:n.1437G>C
|
|
|
ENST00000678404.1:c.987G>C
|
ENSP00000503944.1:p.Gly329=
|
|
ENST00000678419.1:c.987G>C
|
ENSP00000504085.1:p.Gly329=
|
|
ENST00000678433.1:n.1343G>C
|
|
|
ENST00000678467.1:c.987G>C
|
ENSP00000504072.1:p.Gly329=
|
|
ENST00000678569.1:c.983G>C
|
ENSP00000504261.1:p.Gly328Ala
|
|
ENST00000678961.1:n.1342G>C
|
|
|
ENST00000679002.1:n.1166G>C
|
|
|
ENST00000679012.1:c.543G>C
|
ENSP00000504446.1:p.Gly181=
|
|
ENST00000679070.1:c.*406G>C
|
ENSP00000503759.1:n.*406G>C
|
|
ENST00000679130.1:c.987G>C
|
ENSP00000504845.1:p.Gly329=
|
|
ENST00000679315.1:c.*817G>C
|
ENSP00000503065.1:n.*817G>C
|
|
ENST00000243583.10:c.864G>C
|
ENSP00000243583.5:p.Gly288=
|
|
ENST00000324464.7:c.987G>C
|
ENSP00000315118.3:p.Gly329=
|
|
ENST00000593724.1:n.1102G>C
|
|
|
NM_001142555.2:c.864G>C
|
NP_001136027.1:p.Gly288=
|
|
NM_024876.3:c.987G>C
|
NP_079152.3:p.Gly329=
|
|
XM_005259270.3:c.1149G>C
|
XP_005259327.2:p.Gly383=
|
|
XM_005259271.3:c.987G>C
|
XP_005259328.1:p.Gly329=
|
|
XM_005259272.3:c.987G>C
|
XP_005259329.1:p.Gly329=
|
|
XM_005259273.3:c.987G>C
|
XP_005259330.1:p.Gly329=
|
|
XM_006723392.2:c.987G>C
|
XP_006723455.1:p.Gly329=
|
|
XM_006723393.2:c.987G>C
|
XP_006723456.1:p.Gly329=
|
|
XM_011527334.1:c.987G>C
|
XP_011525636.1:p.Gly329=
|
|
XM_011527335.1:c.846G>C
|
XP_011525637.1:p.Gly282=
|
|
XM_011527336.1:c.1017G>C
|
XP_011525638.1:p.Gly339=
|
|
XM_011527337.1:c.987G>C
|
XP_011525639.1:p.Gly329=
|
|
XM_011527338.1:c.987G>C
|
XP_011525640.1:p.Gly329=
|
|
NM_024876.4:c.987G>C
MANE Select
|
NP_079152.3:p.Gly329=
|
|
NM_001142555.3:c.864G>C
|
NP_001136027.1:p.Gly288=
|
|