|
ENST00000377315.6:c.1515G>T
(CACNB2)
|
ENSP00000366532.4:p.Glu505Asp
|
|
|
ENST00000377319.9:c.1380G>T
(CACNB2)
|
ENSP00000366536.3:p.Glu460Asp
|
|
|
ENST00000645287.2:c.1503G>T
(CACNB2)
|
ENSP00000496203.1:p.Glu501Asp
|
|
|
ENST00000282343.13:c.1575G>T
(CACNB2)
|
ENSP00000282343.8:p.Glu525Asp
|
|
|
ENST00000324631.13:c.1659G>T
(CACNB2)
MANE Select
|
ENSP00000320025.8:p.Glu553Asp
|
|
|
ENST00000377315.5:c.1515G>T
(CACNB2)
|
ENSP00000366532.4:p.Glu505Asp
|
|
|
ENST00000377319.8:c.1380G>T
(CACNB2)
|
ENSP00000366536.3:p.Glu460Asp
|
|
|
ENST00000377329.10:c.1497G>T
(CACNB2)
MANE Plus Clinical
|
ENSP00000366546.4:p.Glu499Asp
|
|
|
ENST00000377331.8:c.1284G>T
(CACNB2)
|
ENSP00000366548.4:p.Glu428Asp
|
|
|
ENST00000643096.2:c.1461G>T
(CACNB2)
|
ENSP00000494209.2:p.Glu487Asp
|
|
|
ENST00000645287.1:c.1503G>T
(CACNB2)
|
ENSP00000496203.1:p.Glu501Asp
|
|
|
ENST00000647168.2:c.*800G>T
(CACNB2)
|
ENSP00000495854.2:n.*800G>T
|
|
|
ENST00000650685.1:c.1401G>T
(CACNB2)
|
ENSP00000498460.1:p.Glu467Asp
|
|
|
ENST00000651330.1:c.*933G>T
(CACNB2)
|
ENSP00000498457.1:n.*933G>T
|
|
|
ENST00000651468.1:c.1216G>T
(CACNB2)
|
ENSP00000498352.1:n.1216G>T
|
|
|
ENST00000651928.1:c.*898G>T
(CACNB2)
|
ENSP00000499177.1:n.*898G>T
|
|
|
ENST00000652391.1:c.1479G>T
(CACNB2)
|
ENSP00000498938.1:p.Glu493Asp
|
|
|
ENST00000652478.1:c.*759G>T
(CACNB2)
|
ENSP00000498812.1:n.*759G>T
|
|
|
ENST00000282343.12:c.1575G>T
(CACNB2)
|
ENSP00000282343.8:p.Glu525Asp
|
|
|
ENST00000324631.11:c.1659G>T
(CACNB2)
|
ENSP00000320025.7:p.Glu553Asp
|
|
|
ENST00000352115.10:c.1587G>T
(CACNB2)
|
ENSP00000344474.6:p.Glu529Asp
|
|
|
ENST00000377315.4:c.1515G>T
(CACNB2)
|
ENSP00000366532.4:p.Glu505Asp
|
|
|
ENST00000377319.7:c.1380G>T
(CACNB2)
|
ENSP00000366536.3:p.Glu460Asp
|
|
|
ENST00000377328.5:c.909G>T
(CACNB2)
|
ENSP00000366545.1:p.Glu303Asp
|
|
|
ENST00000377329.8:c.1497G>T
(CACNB2)
|
ENSP00000366546.4:p.Glu499Asp
|
|
|
ENST00000377331.6:c.1503G>T
(CACNB2)
|
ENSP00000366548.2:p.Glu501Asp
|
|
|
ENST00000396576.6:c.1494G>T
(CACNB2)
|
ENSP00000379821.2:p.Glu498Asp
|
|
|
ENST00000612134.4:c.1363G>T
(CACNB2)
|
ENSP00000480563.1:n.1363G>T
|
|
|
ENST00000612743.1:c.171G>T
(CACNB2)
|
ENSP00000478676.1:p.Glu57Asp
|
|
|
ENST00000615785.4:c.744G>T
(CACNB2)
|
ENSP00000480260.1:p.Glu248Asp
|
|
|
ENST00000617363.4:c.1422G>T
(CACNB2)
|
ENSP00000479756.1:p.Glu474Asp
|
|
|
NM_000724.3:c.1494G>T
(CACNB2)
|
NP_000715.2:p.Glu498Asp
|
|
|
NM_001167945.1:c.1461G>T
(CACNB2)
|
NP_001161417.1:p.Glu487Asp
|
|
|
NM_201570.2:c.1515G>T
(CACNB2)
|
NP_963864.1:p.Glu505Asp
|
|
|
NM_201571.3:c.1575G>T
(CACNB2)
|
NP_963865.2:p.Glu525Asp
|
|
|
NM_201572.3:c.1503G>T
(CACNB2)
|
NP_963866.2:p.Glu501Asp
|
|
|
NM_201590.2:c.1497G>T
(CACNB2)
|
NP_963884.2:p.Glu499Asp
|
|
|
NM_201593.2:c.1545G>T
(CACNB2)
|
NP_963887.2:p.Glu515Asp
|
|
|
NM_201596.2:c.1659G>T
(CACNB2)
|
NP_963890.2:p.Glu553Asp
|
|
|
NM_201597.2:c.1587G>T
(CACNB2)
|
NP_963891.1:p.Glu529Asp
|
|
|
XM_005252588.2:c.1401G>T
(CACNB2)
|
XP_005252645.1:p.Glu467Asp
|
|
|
XM_005252591.2:c.819G>T
(CACNB2)
|
XP_005252648.1:p.Glu273Asp
|
|
|
XM_006717502.2:c.1479G>T
(CACNB2)
|
XP_006717565.1:p.Glu493Asp
|
|
|
XM_011519659.1:c.1425G>T
(CACNB2)
|
XP_011517961.1:p.Glu475Asp
|
|
|
XM_011519660.1:c.1380G>T
(CACNB2)
|
XP_011517962.1:p.Glu460Asp
|
|
|
NM_001330060.1:c.1380G>T
(CACNB2)
|
NP_001316989.1:p.Glu460Asp
|
|
|
XM_005252588.4:c.1401G>T
(CACNB2)
|
XP_005252645.1:p.Glu467Asp
|
|
|
XM_005252591.3:c.819G>T
(CACNB2)
|
XP_005252648.1:p.Glu273Asp
|
|
|
XM_006717502.3:c.1479G>T
(CACNB2)
|
XP_006717565.1:p.Glu493Asp
|
|
|
XM_011519659.2:c.1425G>T
(CACNB2)
|
XP_011517961.1:p.Glu475Asp
|
|
|
XM_017016625.1:c.819G>T
(CACNB2)
|
XP_016872114.1:p.Glu273Asp
|
|
|
XR_001747060.1:n.2423+2669C>A
(NSUN6)
|
|
|
|
XR_001747198.1:n.1784G>T
(CACNB2)
|
|
|
|
NM_000724.4:c.1494G>T
(CACNB2)
|
NP_000715.2:p.Glu498Asp
|
|
|
NM_001167945.2:c.1461G>T
(CACNB2)
|
NP_001161417.1:p.Glu487Asp
|
|
|
NM_001330060.2:c.1380G>T
(CACNB2)
|
NP_001316989.1:p.Glu460Asp
|
|
|
NM_201570.3:c.1515G>T
(CACNB2)
|
NP_963864.1:p.Glu505Asp
|
|
|
NM_201571.4:c.1575G>T
(CACNB2)
|
NP_963865.2:p.Glu525Asp
|
|
|
NM_201572.4:c.1503G>T
(CACNB2)
|
NP_963866.2:p.Glu501Asp
|
|
|
NM_201590.3:c.1497G>T
(CACNB2)
MANE Plus Clinical
|
NP_963884.2:p.Glu499Asp
|
|
|
NM_201593.3:c.1545G>T
(CACNB2)
|
NP_963887.2:p.Glu515Asp
|
|
|
NM_201596.3:c.1659G>T
(CACNB2)
MANE Select
|
NP_963890.2:p.Glu553Asp
|
|
|
NM_201597.3:c.1587G>T
(CACNB2)
|
NP_963891.1:p.Glu529Asp
|
|
