ENST00000377315.6:c.1539G>T
(CACNB2)
|
ENSP00000366532.4:p.Glu513Asp
|
|
ENST00000377319.9:c.1404G>T
(CACNB2)
|
ENSP00000366536.3:p.Glu468Asp
|
|
ENST00000645287.2:c.1527G>T
(CACNB2)
|
ENSP00000496203.1:p.Glu509Asp
|
|
ENST00000282343.13:c.1599G>T
(CACNB2)
|
ENSP00000282343.8:p.Glu533Asp
|
|
ENST00000324631.13:c.1683G>T
(CACNB2)
MANE Select
|
ENSP00000320025.8:p.Glu561Asp
|
|
ENST00000377315.5:c.1539G>T
(CACNB2)
|
ENSP00000366532.4:p.Glu513Asp
|
|
ENST00000377319.8:c.1404G>T
(CACNB2)
|
ENSP00000366536.3:p.Glu468Asp
|
|
ENST00000377329.10:c.1521G>T
(CACNB2)
MANE Plus Clinical
|
ENSP00000366546.4:p.Glu507Asp
|
|
ENST00000377331.8:c.1308G>T
(CACNB2)
|
ENSP00000366548.4:p.Glu436Asp
|
|
ENST00000643096.2:c.1485G>T
(CACNB2)
|
ENSP00000494209.2:p.Glu495Asp
|
|
ENST00000645287.1:c.1527G>T
(CACNB2)
|
ENSP00000496203.1:p.Glu509Asp
|
|
ENST00000647168.2:c.*824G>T
(CACNB2)
|
ENSP00000495854.2:n.*824G>T
|
|
ENST00000650685.1:c.1425G>T
(CACNB2)
|
ENSP00000498460.1:p.Glu475Asp
|
|
ENST00000651330.1:c.*957G>T
(CACNB2)
|
ENSP00000498457.1:n.*957G>T
|
|
ENST00000651468.1:c.1240G>T
(CACNB2)
|
ENSP00000498352.1:n.1240G>T
|
|
ENST00000651928.1:c.*922G>T
(CACNB2)
|
ENSP00000499177.1:n.*922G>T
|
|
ENST00000652391.1:c.1503G>T
(CACNB2)
|
ENSP00000498938.1:p.Glu501Asp
|
|
ENST00000652478.1:c.*783G>T
(CACNB2)
|
ENSP00000498812.1:n.*783G>T
|
|
ENST00000282343.12:c.1599G>T
(CACNB2)
|
ENSP00000282343.8:p.Glu533Asp
|
|
ENST00000324631.11:c.1683G>T
(CACNB2)
|
ENSP00000320025.7:p.Glu561Asp
|
|
ENST00000352115.10:c.1611G>T
(CACNB2)
|
ENSP00000344474.6:p.Glu537Asp
|
|
ENST00000377315.4:c.1539G>T
(CACNB2)
|
ENSP00000366532.4:p.Glu513Asp
|
|
ENST00000377319.7:c.1404G>T
(CACNB2)
|
ENSP00000366536.3:p.Glu468Asp
|
|
ENST00000377328.5:c.933G>T
(CACNB2)
|
ENSP00000366545.1:p.Glu311Asp
|
|
ENST00000377329.8:c.1521G>T
(CACNB2)
|
ENSP00000366546.4:p.Glu507Asp
|
|
ENST00000377331.6:c.1527G>T
(CACNB2)
|
ENSP00000366548.2:p.Glu509Asp
|
|
ENST00000396576.6:c.1518G>T
(CACNB2)
|
ENSP00000379821.2:p.Glu506Asp
|
|
ENST00000612134.4:c.1387G>T
(CACNB2)
|
ENSP00000480563.1:n.1387G>T
|
|
ENST00000612743.1:c.195G>T
(CACNB2)
|
ENSP00000478676.1:p.Glu65Asp
|
|
ENST00000615785.4:c.768G>T
(CACNB2)
|
ENSP00000480260.1:p.Glu256Asp
|
|
ENST00000617363.4:c.1446G>T
(CACNB2)
|
ENSP00000479756.1:p.Glu482Asp
|
|
NM_000724.3:c.1518G>T
(CACNB2)
|
NP_000715.2:p.Glu506Asp
|
|
NM_001167945.1:c.1485G>T
(CACNB2)
|
NP_001161417.1:p.Glu495Asp
|
|
NM_201570.2:c.1539G>T
(CACNB2)
|
NP_963864.1:p.Glu513Asp
|
|
NM_201571.3:c.1599G>T
(CACNB2)
|
NP_963865.2:p.Glu533Asp
|
|
NM_201572.3:c.1527G>T
(CACNB2)
|
NP_963866.2:p.Glu509Asp
|
|
NM_201590.2:c.1521G>T
(CACNB2)
|
NP_963884.2:p.Glu507Asp
|
|
NM_201593.2:c.1569G>T
(CACNB2)
|
NP_963887.2:p.Glu523Asp
|
|
NM_201596.2:c.1683G>T
(CACNB2)
|
NP_963890.2:p.Glu561Asp
|
|
NM_201597.2:c.1611G>T
(CACNB2)
|
NP_963891.1:p.Glu537Asp
|
|
XM_005252588.2:c.1425G>T
(CACNB2)
|
XP_005252645.1:p.Glu475Asp
|
|
XM_005252591.2:c.843G>T
(CACNB2)
|
XP_005252648.1:p.Glu281Asp
|
|
XM_006717502.2:c.1503G>T
(CACNB2)
|
XP_006717565.1:p.Glu501Asp
|
|
XM_011519659.1:c.1449G>T
(CACNB2)
|
XP_011517961.1:p.Glu483Asp
|
|
XM_011519660.1:c.1404G>T
(CACNB2)
|
XP_011517962.1:p.Glu468Asp
|
|
NM_001330060.1:c.1404G>T
(CACNB2)
|
NP_001316989.1:p.Glu468Asp
|
|
XM_005252588.4:c.1425G>T
(CACNB2)
|
XP_005252645.1:p.Glu475Asp
|
|
XM_005252591.3:c.843G>T
(CACNB2)
|
XP_005252648.1:p.Glu281Asp
|
|
XM_006717502.3:c.1503G>T
(CACNB2)
|
XP_006717565.1:p.Glu501Asp
|
|
XM_011519659.2:c.1449G>T
(CACNB2)
|
XP_011517961.1:p.Glu483Asp
|
|
XM_017016625.1:c.843G>T
(CACNB2)
|
XP_016872114.1:p.Glu281Asp
|
|
XR_001747060.1:n.2423+2645C>A
(NSUN6)
|
|
|
XR_001747198.1:n.1808G>T
(CACNB2)
|
|
|
NM_000724.4:c.1518G>T
(CACNB2)
|
NP_000715.2:p.Glu506Asp
|
|
NM_001167945.2:c.1485G>T
(CACNB2)
|
NP_001161417.1:p.Glu495Asp
|
|
NM_001330060.2:c.1404G>T
(CACNB2)
|
NP_001316989.1:p.Glu468Asp
|
|
NM_201570.3:c.1539G>T
(CACNB2)
|
NP_963864.1:p.Glu513Asp
|
|
NM_201571.4:c.1599G>T
(CACNB2)
|
NP_963865.2:p.Glu533Asp
|
|
NM_201572.4:c.1527G>T
(CACNB2)
|
NP_963866.2:p.Glu509Asp
|
|
NM_201590.3:c.1521G>T
(CACNB2)
MANE Plus Clinical
|
NP_963884.2:p.Glu507Asp
|
|
NM_201593.3:c.1569G>T
(CACNB2)
|
NP_963887.2:p.Glu523Asp
|
|
NM_201596.3:c.1683G>T
(CACNB2)
MANE Select
|
NP_963890.2:p.Glu561Asp
|
|
NM_201597.3:c.1611G>T
(CACNB2)
|
NP_963891.1:p.Glu537Asp
|
|