ENST00000377315.6:c.1551T>G
(CACNB2)
|
ENSP00000366532.4:p.Ser517=
|
|
ENST00000377319.9:c.1416T>G
(CACNB2)
|
ENSP00000366536.3:p.Ser472=
|
|
ENST00000645287.2:c.1539T>G
(CACNB2)
|
ENSP00000496203.1:p.Ser513=
|
|
ENST00000282343.13:c.1611T>G
(CACNB2)
|
ENSP00000282343.8:p.Ser537=
|
|
ENST00000324631.13:c.1695T>G
(CACNB2)
MANE Select
|
ENSP00000320025.8:p.Ser565=
|
|
ENST00000377315.5:c.1551T>G
(CACNB2)
|
ENSP00000366532.4:p.Ser517=
|
|
ENST00000377319.8:c.1416T>G
(CACNB2)
|
ENSP00000366536.3:p.Ser472=
|
|
ENST00000377329.10:c.1533T>G
(CACNB2)
MANE Plus Clinical
|
ENSP00000366546.4:p.Ser511=
|
|
ENST00000377331.8:c.1320T>G
(CACNB2)
|
ENSP00000366548.4:p.Ser440=
|
|
ENST00000643096.2:c.1497T>G
(CACNB2)
|
ENSP00000494209.2:p.Ser499=
|
|
ENST00000645287.1:c.1539T>G
(CACNB2)
|
ENSP00000496203.1:p.Ser513=
|
|
ENST00000647168.2:c.*836T>G
(CACNB2)
|
ENSP00000495854.2:n.*836T>G
|
|
ENST00000650685.1:c.1437T>G
(CACNB2)
|
ENSP00000498460.1:p.Ser479=
|
|
ENST00000651330.1:c.*969T>G
(CACNB2)
|
ENSP00000498457.1:n.*969T>G
|
|
ENST00000651468.1:c.1252T>G
(CACNB2)
|
ENSP00000498352.1:n.1252T>G
|
|
ENST00000651928.1:c.*934T>G
(CACNB2)
|
ENSP00000499177.1:n.*934T>G
|
|
ENST00000652391.1:c.1515T>G
(CACNB2)
|
ENSP00000498938.1:p.Ser505=
|
|
ENST00000652478.1:c.*795T>G
(CACNB2)
|
ENSP00000498812.1:n.*795T>G
|
|
ENST00000282343.12:c.1611T>G
(CACNB2)
|
ENSP00000282343.8:p.Ser537=
|
|
ENST00000324631.11:c.1695T>G
(CACNB2)
|
ENSP00000320025.7:p.Ser565=
|
|
ENST00000352115.10:c.1623T>G
(CACNB2)
|
ENSP00000344474.6:p.Ser541=
|
|
ENST00000377315.4:c.1551T>G
(CACNB2)
|
ENSP00000366532.4:p.Ser517=
|
|
ENST00000377319.7:c.1416T>G
(CACNB2)
|
ENSP00000366536.3:p.Ser472=
|
|
ENST00000377328.5:c.945T>G
(CACNB2)
|
ENSP00000366545.1:p.Ser315=
|
|
ENST00000377329.8:c.1533T>G
(CACNB2)
|
ENSP00000366546.4:p.Ser511=
|
|
ENST00000377331.6:c.1539T>G
(CACNB2)
|
ENSP00000366548.2:p.Ser513=
|
|
ENST00000396576.6:c.1530T>G
(CACNB2)
|
ENSP00000379821.2:p.Ser510=
|
|
ENST00000612134.4:c.1399T>G
(CACNB2)
|
ENSP00000480563.1:n.1399T>G
|
|
ENST00000612743.1:c.207T>G
(CACNB2)
|
ENSP00000478676.1:p.Ser69=
|
|
ENST00000615785.4:c.780T>G
(CACNB2)
|
ENSP00000480260.1:p.Ser260=
|
|
ENST00000617363.4:c.1458T>G
(CACNB2)
|
ENSP00000479756.1:p.Ser486=
|
|
NM_000724.3:c.1530T>G
(CACNB2)
|
NP_000715.2:p.Ser510=
|
|
NM_001167945.1:c.1497T>G
(CACNB2)
|
NP_001161417.1:p.Ser499=
|
|
NM_201570.2:c.1551T>G
(CACNB2)
|
NP_963864.1:p.Ser517=
|
|
NM_201571.3:c.1611T>G
(CACNB2)
|
NP_963865.2:p.Ser537=
|
|
NM_201572.3:c.1539T>G
(CACNB2)
|
NP_963866.2:p.Ser513=
|
|
NM_201590.2:c.1533T>G
(CACNB2)
|
NP_963884.2:p.Ser511=
|
|
NM_201593.2:c.1581T>G
(CACNB2)
|
NP_963887.2:p.Ser527=
|
|
NM_201596.2:c.1695T>G
(CACNB2)
|
NP_963890.2:p.Ser565=
|
|
NM_201597.2:c.1623T>G
(CACNB2)
|
NP_963891.1:p.Ser541=
|
|
XM_005252588.2:c.1437T>G
(CACNB2)
|
XP_005252645.1:p.Ser479=
|
|
XM_005252591.2:c.855T>G
(CACNB2)
|
XP_005252648.1:p.Ser285=
|
|
XM_006717502.2:c.1515T>G
(CACNB2)
|
XP_006717565.1:p.Ser505=
|
|
XM_011519659.1:c.1461T>G
(CACNB2)
|
XP_011517961.1:p.Ser487=
|
|
XM_011519660.1:c.1416T>G
(CACNB2)
|
XP_011517962.1:p.Ser472=
|
|
NM_001330060.1:c.1416T>G
(CACNB2)
|
NP_001316989.1:p.Ser472=
|
|
XM_005252588.4:c.1437T>G
(CACNB2)
|
XP_005252645.1:p.Ser479=
|
|
XM_005252591.3:c.855T>G
(CACNB2)
|
XP_005252648.1:p.Ser285=
|
|
XM_006717502.3:c.1515T>G
(CACNB2)
|
XP_006717565.1:p.Ser505=
|
|
XM_011519659.2:c.1461T>G
(CACNB2)
|
XP_011517961.1:p.Ser487=
|
|
XM_017016625.1:c.855T>G
(CACNB2)
|
XP_016872114.1:p.Ser285=
|
|
XR_001747060.1:n.2423+2633A>C
(NSUN6)
|
|
|
XR_001747198.1:n.1820T>G
(CACNB2)
|
|
|
NM_000724.4:c.1530T>G
(CACNB2)
|
NP_000715.2:p.Ser510=
|
|
NM_001167945.2:c.1497T>G
(CACNB2)
|
NP_001161417.1:p.Ser499=
|
|
NM_001330060.2:c.1416T>G
(CACNB2)
|
NP_001316989.1:p.Ser472=
|
|
NM_201570.3:c.1551T>G
(CACNB2)
|
NP_963864.1:p.Ser517=
|
|
NM_201571.4:c.1611T>G
(CACNB2)
|
NP_963865.2:p.Ser537=
|
|
NM_201572.4:c.1539T>G
(CACNB2)
|
NP_963866.2:p.Ser513=
|
|
NM_201590.3:c.1533T>G
(CACNB2)
MANE Plus Clinical
|
NP_963884.2:p.Ser511=
|
|
NM_201593.3:c.1581T>G
(CACNB2)
|
NP_963887.2:p.Ser527=
|
|
NM_201596.3:c.1695T>G
(CACNB2)
MANE Select
|
NP_963890.2:p.Ser565=
|
|
NM_201597.3:c.1623T>G
(CACNB2)
|
NP_963891.1:p.Ser541=
|
|