ENST00000377315.6:c.1470C>T
(CACNB2)
|
ENSP00000366532.4:p.His490=
|
|
ENST00000377319.9:c.1335C>T
(CACNB2)
|
ENSP00000366536.3:p.His445=
|
|
ENST00000645287.2:c.1458C>T
(CACNB2)
|
ENSP00000496203.1:p.His486=
|
|
ENST00000282343.13:c.1530C>T
(CACNB2)
|
ENSP00000282343.8:p.His510=
|
|
ENST00000324631.13:c.1614C>T
(CACNB2)
MANE Select
|
ENSP00000320025.8:p.His538=
|
|
ENST00000377315.5:c.1470C>T
(CACNB2)
|
ENSP00000366532.4:p.His490=
|
|
ENST00000377319.8:c.1335C>T
(CACNB2)
|
ENSP00000366536.3:p.His445=
|
|
ENST00000377329.10:c.1452C>T
(CACNB2)
MANE Plus Clinical
|
ENSP00000366546.4:p.His484=
|
|
ENST00000377331.8:c.1239C>T
(CACNB2)
|
ENSP00000366548.4:p.His413=
|
|
ENST00000643096.2:c.1416C>T
(CACNB2)
|
ENSP00000494209.2:p.His472=
|
|
ENST00000645287.1:c.1458C>T
(CACNB2)
|
ENSP00000496203.1:p.His486=
|
|
ENST00000647168.2:c.*755C>T
(CACNB2)
|
ENSP00000495854.2:n.*755C>T
|
|
ENST00000650685.1:c.1356C>T
(CACNB2)
|
ENSP00000498460.1:p.His452=
|
|
ENST00000651330.1:c.*888C>T
(CACNB2)
|
ENSP00000498457.1:n.*888C>T
|
|
ENST00000651468.1:c.1171C>T
(CACNB2)
|
ENSP00000498352.1:n.1171C>T
|
|
ENST00000651928.1:c.*853C>T
(CACNB2)
|
ENSP00000499177.1:n.*853C>T
|
|
ENST00000652391.1:c.1434C>T
(CACNB2)
|
ENSP00000498938.1:p.His478=
|
|
ENST00000652478.1:c.*714C>T
(CACNB2)
|
ENSP00000498812.1:n.*714C>T
|
|
ENST00000282343.12:c.1530C>T
(CACNB2)
|
ENSP00000282343.8:p.His510=
|
|
ENST00000324631.11:c.1614C>T
(CACNB2)
|
ENSP00000320025.7:p.His538=
|
|
ENST00000352115.10:c.1542C>T
(CACNB2)
|
ENSP00000344474.6:p.His514=
|
|
ENST00000377315.4:c.1470C>T
(CACNB2)
|
ENSP00000366532.4:p.His490=
|
|
ENST00000377319.7:c.1335C>T
(CACNB2)
|
ENSP00000366536.3:p.His445=
|
|
ENST00000377328.5:c.864C>T
(CACNB2)
|
ENSP00000366545.1:p.His288=
|
|
ENST00000377329.8:c.1452C>T
(CACNB2)
|
ENSP00000366546.4:p.His484=
|
|
ENST00000377331.6:c.1458C>T
(CACNB2)
|
ENSP00000366548.2:p.His486=
|
|
ENST00000396576.6:c.1449C>T
(CACNB2)
|
ENSP00000379821.2:p.His483=
|
|
ENST00000612134.4:c.1318C>T
(CACNB2)
|
ENSP00000480563.1:n.1318C>T
|
|
ENST00000612743.1:c.126C>T
(CACNB2)
|
ENSP00000478676.1:p.His42=
|
|
ENST00000615785.4:c.699C>T
(CACNB2)
|
ENSP00000480260.1:p.His233=
|
|
ENST00000617363.4:c.1377C>T
(CACNB2)
|
ENSP00000479756.1:p.His459=
|
|
NM_000724.3:c.1449C>T
(CACNB2)
|
NP_000715.2:p.His483=
|
|
NM_001167945.1:c.1416C>T
(CACNB2)
|
NP_001161417.1:p.His472=
|
|
NM_201570.2:c.1470C>T
(CACNB2)
|
NP_963864.1:p.His490=
|
|
NM_201571.3:c.1530C>T
(CACNB2)
|
NP_963865.2:p.His510=
|
|
NM_201572.3:c.1458C>T
(CACNB2)
|
NP_963866.2:p.His486=
|
|
NM_201590.2:c.1452C>T
(CACNB2)
|
NP_963884.2:p.His484=
|
|
NM_201593.2:c.1500C>T
(CACNB2)
|
NP_963887.2:p.His500=
|
|
NM_201596.2:c.1614C>T
(CACNB2)
|
NP_963890.2:p.His538=
|
|
NM_201597.2:c.1542C>T
(CACNB2)
|
NP_963891.1:p.His514=
|
|
XM_005252588.2:c.1356C>T
(CACNB2)
|
XP_005252645.1:p.His452=
|
|
XM_005252591.2:c.774C>T
(CACNB2)
|
XP_005252648.1:p.His258=
|
|
XM_006717502.2:c.1434C>T
(CACNB2)
|
XP_006717565.1:p.His478=
|
|
XM_011519659.1:c.1380C>T
(CACNB2)
|
XP_011517961.1:p.His460=
|
|
XM_011519660.1:c.1335C>T
(CACNB2)
|
XP_011517962.1:p.His445=
|
|
NM_001330060.1:c.1335C>T
(CACNB2)
|
NP_001316989.1:p.His445=
|
|
XM_005252588.4:c.1356C>T
(CACNB2)
|
XP_005252645.1:p.His452=
|
|
XM_005252591.3:c.774C>T
(CACNB2)
|
XP_005252648.1:p.His258=
|
|
XM_006717502.3:c.1434C>T
(CACNB2)
|
XP_006717565.1:p.His478=
|
|
XM_011519659.2:c.1380C>T
(CACNB2)
|
XP_011517961.1:p.His460=
|
|
XM_017016625.1:c.774C>T
(CACNB2)
|
XP_016872114.1:p.His258=
|
|
XR_001747060.1:n.2423+2714G>A
(NSUN6)
|
|
|
XR_001747198.1:n.1739C>T
(CACNB2)
|
|
|
NM_000724.4:c.1449C>T
(CACNB2)
|
NP_000715.2:p.His483=
|
|
NM_001167945.2:c.1416C>T
(CACNB2)
|
NP_001161417.1:p.His472=
|
|
NM_001330060.2:c.1335C>T
(CACNB2)
|
NP_001316989.1:p.His445=
|
|
NM_201570.3:c.1470C>T
(CACNB2)
|
NP_963864.1:p.His490=
|
|
NM_201571.4:c.1530C>T
(CACNB2)
|
NP_963865.2:p.His510=
|
|
NM_201572.4:c.1458C>T
(CACNB2)
|
NP_963866.2:p.His486=
|
|
NM_201590.3:c.1452C>T
(CACNB2)
MANE Plus Clinical
|
NP_963884.2:p.His484=
|
|
NM_201593.3:c.1500C>T
(CACNB2)
|
NP_963887.2:p.His500=
|
|
NM_201596.3:c.1614C>T
(CACNB2)
MANE Select
|
NP_963890.2:p.His538=
|
|
NM_201597.3:c.1542C>T
(CACNB2)
|
NP_963891.1:p.His514=
|
|