|
ENST00000380834.7:c.*659A>G
(CENPO)
MANE Select
|
ENSP00000370214.2:n.*659A>G
|
|
|
ENST00000405392.6:c.3393T>C
(ADCY3)
|
ENSP00000384484.2:p.Asn1131=
|
|
|
ENST00000679454.1:c.3390T>C
(ADCY3)
MANE Select
|
ENSP00000505261.1:p.Asn1130=
|
|
|
ENST00000260600.9:c.3390T>C
(ADCY3)
|
ENSP00000260600.5:p.Asn1130=
|
|
|
ENST00000260662.2:c.*659A>G
(CENPO)
|
ENSP00000260662.1:n.*659A>G
|
|
|
ENST00000380834.6:c.*659A>G
(CENPO)
|
ENSP00000370214.2:n.*659A>G
|
|
|
ENST00000405392.5:c.3393T>C
(ADCY3)
|
ENSP00000384484.2:p.Asn1131=
|
|
|
ENST00000473706.5:c.*659A>G
(CENPO)
|
ENSP00000417787.1:n.*659A>G
|
|
|
ENST00000498288.1:c.279T>C
(ADCY3)
|
|
|
|
ENST00000606682.5:c.2331T>C
(ADCY3)
|
ENSP00000475652.1:p.Asn777=
|
|
|
NM_001199803.1:c.*659A>G
(CENPO)
|
NP_001186732.1:n.*659A>G
|
|
|
NM_004036.3:c.3390T>C
(ADCY3)
|
NP_004027.2:p.Asn1130=
|
|
|
NM_024322.2:c.*659A>G
(CENPO)
|
NP_077298.1:n.*659A>G
|
|
|
XM_005264104.1:c.3393T>C
(ADCY3)
|
XP_005264161.1:p.Asn1131=
|
|
|
XM_005264105.1:c.3390T>C
(ADCY3)
|
XP_005264162.1:p.Asn1130=
|
|
|
XM_006711925.1:c.3459T>C
(ADCY3)
|
XP_006711988.1:p.Asn1153=
|
|
|
XM_011532489.1:c.3516T>C
(ADCY3)
|
XP_011530791.1:p.Asn1172=
|
|
|
XM_011532490.1:c.3513T>C
(ADCY3)
|
XP_011530792.1:p.Asn1171=
|
|
|
XM_011532491.1:c.3450T>C
(ADCY3)
|
XP_011530793.1:p.Asn1150=
|
|
|
XM_011532493.1:c.3378T>C
(ADCY3)
|
XP_011530795.1:p.Asn1126=
|
|
|
XM_011532494.1:c.3318T>C
(ADCY3)
|
XP_011530796.1:p.Asn1106=
|
|
|
XM_011532495.1:c.2850T>C
(ADCY3)
|
XP_011530797.1:p.Asn950=
|
|
|
XM_011532496.1:c.2793T>C
(ADCY3)
|
XP_011530798.1:p.Asn931=
|
|
|
NM_001199803.2:c.*659A>G
(CENPO)
|
NP_001186732.1:n.*659A>G
|
|
|
NM_001320613.1:c.3393T>C
(ADCY3)
|
NP_001307542.1:p.Asn1131=
|
|
|
NM_001322101.1:c.*659A>G
(CENPO)
|
NP_001309030.1:n.*659A>G
|
|
|
NM_004036.4:c.3390T>C
(ADCY3)
|
NP_004027.2:p.Asn1130=
|
|
|
NM_024322.3:c.*659A>G
(CENPO)
|
NP_077298.1:n.*659A>G
|
|
|
NR_136182.1:n.1821A>G
(CENPO)
|
|
|
|
NR_136183.1:n.1922A>G
(CENPO)
|
|
|
|
NR_136184.1:n.1802A>G
(CENPO)
|
|
|
|
XM_011532492.2:c.*131T>C
(ADCY3)
|
XP_011530794.1:n.*131T>C
|
|
|
XM_017003186.1:c.3456T>C
(ADCY3)
|
XP_016858675.1:p.Asn1152=
|
|
|
XM_017003187.1:c.3447T>C
(ADCY3)
|
XP_016858676.1:p.Asn1149=
|
|
|
XM_017003188.1:c.*131T>C
(ADCY3)
|
XP_016858677.1:n.*131T>C
|
|
|
XM_017003189.1:c.3375T>C
(ADCY3)
|
XP_016858678.1:p.Asn1125=
|
|
|
XM_017003190.1:c.3252T>C
(ADCY3)
|
XP_016858679.1:p.Asn1084=
|
|
|
XM_017003191.1:c.2880T>C
(ADCY3)
|
XP_016858680.1:p.Asn960=
|
|
|
XM_017003192.1:c.2670T>C
(ADCY3)
|
XP_016858681.1:p.Asn890=
|
|
|
XM_017003193.1:c.2667T>C
(ADCY3)
|
XP_016858682.1:p.Asn889=
|
|
|
NM_001322101.2:c.*659A>G
(CENPO)
MANE Select
|
NP_001309030.1:n.*659A>G
|
|
|
NM_001199803.3:c.*659A>G
(CENPO)
|
NP_001186732.1:n.*659A>G
|
|
|
NM_001320613.2:c.3393T>C
(ADCY3)
|
NP_001307542.1:p.Asn1131=
|
|
|
NM_001377128.1:c.3456T>C
(ADCY3)
|
NP_001364057.1:p.Asn1152=
|
|
|
NM_001377129.1:c.3252T>C
(ADCY3)
|
NP_001364058.1:p.Asn1084=
|
|
|
NM_001377130.1:c.*131T>C
(ADCY3)
|
NP_001364059.1:n.*131T>C
|
|
|
NM_001377131.1:c.2667T>C
(ADCY3)
|
NP_001364060.1:p.Asn889=
|
|
|
NM_001377132.1:c.3390T>C
(ADCY3)
|
NP_001364061.1:p.Asn1130=
|
|
|
NM_004036.5:c.3390T>C
(ADCY3)
MANE Select
|
NP_004027.2:p.Asn1130=
|
|
|
NR_136182.2:n.1511A>G
(CENPO)
|
|
|
|
NR_136183.2:n.1612A>G
(CENPO)
|
|
|
|
NR_136184.2:n.1492A>G
(CENPO)
|
|
|
|
NM_024322.4:c.*659A>G
(CENPO)
|
NP_077298.1:n.*659A>G
|
|
