|
ENST00000377315.6:c.1485T>A
(CACNB2)
|
ENSP00000366532.4:p.Ser495Arg
|
|
|
ENST00000377319.9:c.1350T>A
(CACNB2)
|
ENSP00000366536.3:p.Ser450Arg
|
|
|
ENST00000645287.2:c.1473T>A
(CACNB2)
|
ENSP00000496203.1:p.Ser491Arg
|
|
|
ENST00000282343.13:c.1545T>A
(CACNB2)
|
ENSP00000282343.8:p.Ser515Arg
|
|
|
ENST00000324631.13:c.1629T>A
(CACNB2)
MANE Select
|
ENSP00000320025.8:p.Ser543Arg
|
|
|
ENST00000377315.5:c.1485T>A
(CACNB2)
|
ENSP00000366532.4:p.Ser495Arg
|
|
|
ENST00000377319.8:c.1350T>A
(CACNB2)
|
ENSP00000366536.3:p.Ser450Arg
|
|
|
ENST00000377329.10:c.1467T>A
(CACNB2)
MANE Plus Clinical
|
ENSP00000366546.4:p.Ser489Arg
|
|
|
ENST00000377331.8:c.1254T>A
(CACNB2)
|
ENSP00000366548.4:p.Ser418Arg
|
|
|
ENST00000643096.2:c.1431T>A
(CACNB2)
|
ENSP00000494209.2:p.Ser477Arg
|
|
|
ENST00000645287.1:c.1473T>A
(CACNB2)
|
ENSP00000496203.1:p.Ser491Arg
|
|
|
ENST00000647168.2:c.*770T>A
(CACNB2)
|
ENSP00000495854.2:n.*770T>A
|
|
|
ENST00000650685.1:c.1371T>A
(CACNB2)
|
ENSP00000498460.1:p.Ser457Arg
|
|
|
ENST00000651330.1:c.*903T>A
(CACNB2)
|
ENSP00000498457.1:n.*903T>A
|
|
|
ENST00000651468.1:c.1186T>A
(CACNB2)
|
ENSP00000498352.1:n.1186T>A
|
|
|
ENST00000651928.1:c.*868T>A
(CACNB2)
|
ENSP00000499177.1:n.*868T>A
|
|
|
ENST00000652391.1:c.1449T>A
(CACNB2)
|
ENSP00000498938.1:p.Ser483Arg
|
|
|
ENST00000652478.1:c.*729T>A
(CACNB2)
|
ENSP00000498812.1:n.*729T>A
|
|
|
ENST00000282343.12:c.1545T>A
(CACNB2)
|
ENSP00000282343.8:p.Ser515Arg
|
|
|
ENST00000324631.11:c.1629T>A
(CACNB2)
|
ENSP00000320025.7:p.Ser543Arg
|
|
|
ENST00000352115.10:c.1557T>A
(CACNB2)
|
ENSP00000344474.6:p.Ser519Arg
|
|
|
ENST00000377315.4:c.1485T>A
(CACNB2)
|
ENSP00000366532.4:p.Ser495Arg
|
|
|
ENST00000377319.7:c.1350T>A
(CACNB2)
|
ENSP00000366536.3:p.Ser450Arg
|
|
|
ENST00000377328.5:c.879T>A
(CACNB2)
|
ENSP00000366545.1:p.Ser293Arg
|
|
|
ENST00000377329.8:c.1467T>A
(CACNB2)
|
ENSP00000366546.4:p.Ser489Arg
|
|
|
ENST00000377331.6:c.1473T>A
(CACNB2)
|
ENSP00000366548.2:p.Ser491Arg
|
|
|
ENST00000396576.6:c.1464T>A
(CACNB2)
|
ENSP00000379821.2:p.Ser488Arg
|
|
|
ENST00000612134.4:c.1333T>A
(CACNB2)
|
ENSP00000480563.1:n.1333T>A
|
|
|
ENST00000612743.1:c.141T>A
(CACNB2)
|
ENSP00000478676.1:p.Ser47Arg
|
|
|
ENST00000615785.4:c.714T>A
(CACNB2)
|
ENSP00000480260.1:p.Ser238Arg
|
|
|
ENST00000617363.4:c.1392T>A
(CACNB2)
|
ENSP00000479756.1:p.Ser464Arg
|
|
|
NM_000724.3:c.1464T>A
(CACNB2)
|
NP_000715.2:p.Ser488Arg
|
|
|
NM_001167945.1:c.1431T>A
(CACNB2)
|
NP_001161417.1:p.Ser477Arg
|
|
|
NM_201570.2:c.1485T>A
(CACNB2)
|
NP_963864.1:p.Ser495Arg
|
|
|
NM_201571.3:c.1545T>A
(CACNB2)
|
NP_963865.2:p.Ser515Arg
|
|
|
NM_201572.3:c.1473T>A
(CACNB2)
|
NP_963866.2:p.Ser491Arg
|
|
|
NM_201590.2:c.1467T>A
(CACNB2)
|
NP_963884.2:p.Ser489Arg
|
|
|
NM_201593.2:c.1515T>A
(CACNB2)
|
NP_963887.2:p.Ser505Arg
|
|
|
NM_201596.2:c.1629T>A
(CACNB2)
|
NP_963890.2:p.Ser543Arg
|
|
|
NM_201597.2:c.1557T>A
(CACNB2)
|
NP_963891.1:p.Ser519Arg
|
|
|
XM_005252588.2:c.1371T>A
(CACNB2)
|
XP_005252645.1:p.Ser457Arg
|
|
|
XM_005252591.2:c.789T>A
(CACNB2)
|
XP_005252648.1:p.Ser263Arg
|
|
|
XM_006717502.2:c.1449T>A
(CACNB2)
|
XP_006717565.1:p.Ser483Arg
|
|
|
XM_011519659.1:c.1395T>A
(CACNB2)
|
XP_011517961.1:p.Ser465Arg
|
|
|
XM_011519660.1:c.1350T>A
(CACNB2)
|
XP_011517962.1:p.Ser450Arg
|
|
|
NM_001330060.1:c.1350T>A
(CACNB2)
|
NP_001316989.1:p.Ser450Arg
|
|
|
XM_005252588.4:c.1371T>A
(CACNB2)
|
XP_005252645.1:p.Ser457Arg
|
|
|
XM_005252591.3:c.789T>A
(CACNB2)
|
XP_005252648.1:p.Ser263Arg
|
|
|
XM_006717502.3:c.1449T>A
(CACNB2)
|
XP_006717565.1:p.Ser483Arg
|
|
|
XM_011519659.2:c.1395T>A
(CACNB2)
|
XP_011517961.1:p.Ser465Arg
|
|
|
XM_017016625.1:c.789T>A
(CACNB2)
|
XP_016872114.1:p.Ser263Arg
|
|
|
XR_001747060.1:n.2423+2699A>T
(NSUN6)
|
|
|
|
XR_001747198.1:n.1754T>A
(CACNB2)
|
|
|
|
NM_000724.4:c.1464T>A
(CACNB2)
|
NP_000715.2:p.Ser488Arg
|
|
|
NM_001167945.2:c.1431T>A
(CACNB2)
|
NP_001161417.1:p.Ser477Arg
|
|
|
NM_001330060.2:c.1350T>A
(CACNB2)
|
NP_001316989.1:p.Ser450Arg
|
|
|
NM_201570.3:c.1485T>A
(CACNB2)
|
NP_963864.1:p.Ser495Arg
|
|
|
NM_201571.4:c.1545T>A
(CACNB2)
|
NP_963865.2:p.Ser515Arg
|
|
|
NM_201572.4:c.1473T>A
(CACNB2)
|
NP_963866.2:p.Ser491Arg
|
|
|
NM_201590.3:c.1467T>A
(CACNB2)
MANE Plus Clinical
|
NP_963884.2:p.Ser489Arg
|
|
|
NM_201593.3:c.1515T>A
(CACNB2)
|
NP_963887.2:p.Ser505Arg
|
|
|
NM_201596.3:c.1629T>A
(CACNB2)
MANE Select
|
NP_963890.2:p.Ser543Arg
|
|
|
NM_201597.3:c.1557T>A
(CACNB2)
|
NP_963891.1:p.Ser519Arg
|
|
