|
ENST00000377315.6:c.1557C>A
(CACNB2)
|
ENSP00000366532.4:p.Tyr519Ter
|
|
|
ENST00000377319.9:c.1422C>A
(CACNB2)
|
ENSP00000366536.3:p.Tyr474Ter
|
|
|
ENST00000645287.2:c.1545C>A
(CACNB2)
|
ENSP00000496203.1:p.Tyr515Ter
|
|
|
ENST00000282343.13:c.1617C>A
(CACNB2)
|
ENSP00000282343.8:p.Tyr539Ter
|
|
|
ENST00000324631.13:c.1701C>A
(CACNB2)
MANE Select
|
ENSP00000320025.8:p.Tyr567Ter
|
|
|
ENST00000377315.5:c.1557C>A
(CACNB2)
|
ENSP00000366532.4:p.Tyr519Ter
|
|
|
ENST00000377319.8:c.1422C>A
(CACNB2)
|
ENSP00000366536.3:p.Tyr474Ter
|
|
|
ENST00000377329.10:c.1539C>A
(CACNB2)
MANE Plus Clinical
|
ENSP00000366546.4:p.Tyr513Ter
|
|
|
ENST00000377331.8:c.1326C>A
(CACNB2)
|
ENSP00000366548.4:p.Tyr442Ter
|
|
|
ENST00000643096.2:c.1503C>A
(CACNB2)
|
ENSP00000494209.2:p.Tyr501Ter
|
|
|
ENST00000645287.1:c.1545C>A
(CACNB2)
|
ENSP00000496203.1:p.Tyr515Ter
|
|
|
ENST00000647168.2:c.*842C>A
(CACNB2)
|
ENSP00000495854.2:n.*842C>A
|
|
|
ENST00000650685.1:c.1443C>A
(CACNB2)
|
ENSP00000498460.1:p.Tyr481Ter
|
|
|
ENST00000651330.1:c.*975C>A
(CACNB2)
|
ENSP00000498457.1:n.*975C>A
|
|
|
ENST00000651468.1:c.1258C>A
(CACNB2)
|
ENSP00000498352.1:n.1258C>A
|
|
|
ENST00000651928.1:c.*940C>A
(CACNB2)
|
ENSP00000499177.1:n.*940C>A
|
|
|
ENST00000652391.1:c.1521C>A
(CACNB2)
|
ENSP00000498938.1:p.Tyr507Ter
|
|
|
ENST00000652478.1:c.*801C>A
(CACNB2)
|
ENSP00000498812.1:n.*801C>A
|
|
|
ENST00000282343.12:c.1617C>A
(CACNB2)
|
ENSP00000282343.8:p.Tyr539Ter
|
|
|
ENST00000324631.11:c.1701C>A
(CACNB2)
|
ENSP00000320025.7:p.Tyr567Ter
|
|
|
ENST00000352115.10:c.1629C>A
(CACNB2)
|
ENSP00000344474.6:p.Tyr543Ter
|
|
|
ENST00000377315.4:c.1557C>A
(CACNB2)
|
ENSP00000366532.4:p.Tyr519Ter
|
|
|
ENST00000377319.7:c.1422C>A
(CACNB2)
|
ENSP00000366536.3:p.Tyr474Ter
|
|
|
ENST00000377328.5:c.951C>A
(CACNB2)
|
ENSP00000366545.1:p.Tyr317Ter
|
|
|
ENST00000377329.8:c.1539C>A
(CACNB2)
|
ENSP00000366546.4:p.Tyr513Ter
|
|
|
ENST00000377331.6:c.1545C>A
(CACNB2)
|
ENSP00000366548.2:p.Tyr515Ter
|
|
|
ENST00000396576.6:c.1536C>A
(CACNB2)
|
ENSP00000379821.2:p.Tyr512Ter
|
|
|
ENST00000612134.4:c.1405C>A
(CACNB2)
|
ENSP00000480563.1:n.1405C>A
|
|
|
ENST00000612743.1:c.213C>A
(CACNB2)
|
ENSP00000478676.1:p.Tyr71Ter
|
|
|
ENST00000615785.4:c.786C>A
(CACNB2)
|
ENSP00000480260.1:p.Tyr262Ter
|
|
|
ENST00000617363.4:c.1464C>A
(CACNB2)
|
ENSP00000479756.1:p.Tyr488Ter
|
|
|
NM_000724.3:c.1536C>A
(CACNB2)
|
NP_000715.2:p.Tyr512Ter
|
|
|
NM_001167945.1:c.1503C>A
(CACNB2)
|
NP_001161417.1:p.Tyr501Ter
|
|
|
NM_201570.2:c.1557C>A
(CACNB2)
|
NP_963864.1:p.Tyr519Ter
|
|
|
NM_201571.3:c.1617C>A
(CACNB2)
|
NP_963865.2:p.Tyr539Ter
|
|
|
NM_201572.3:c.1545C>A
(CACNB2)
|
NP_963866.2:p.Tyr515Ter
|
|
|
NM_201590.2:c.1539C>A
(CACNB2)
|
NP_963884.2:p.Tyr513Ter
|
|
|
NM_201593.2:c.1587C>A
(CACNB2)
|
NP_963887.2:p.Tyr529Ter
|
|
|
NM_201596.2:c.1701C>A
(CACNB2)
|
NP_963890.2:p.Tyr567Ter
|
|
|
NM_201597.2:c.1629C>A
(CACNB2)
|
NP_963891.1:p.Tyr543Ter
|
|
|
XM_005252588.2:c.1443C>A
(CACNB2)
|
XP_005252645.1:p.Tyr481Ter
|
|
|
XM_005252591.2:c.861C>A
(CACNB2)
|
XP_005252648.1:p.Tyr287Ter
|
|
|
XM_006717502.2:c.1521C>A
(CACNB2)
|
XP_006717565.1:p.Tyr507Ter
|
|
|
XM_011519659.1:c.1467C>A
(CACNB2)
|
XP_011517961.1:p.Tyr489Ter
|
|
|
XM_011519660.1:c.1422C>A
(CACNB2)
|
XP_011517962.1:p.Tyr474Ter
|
|
|
NM_001330060.1:c.1422C>A
(CACNB2)
|
NP_001316989.1:p.Tyr474Ter
|
|
|
XM_005252588.4:c.1443C>A
(CACNB2)
|
XP_005252645.1:p.Tyr481Ter
|
|
|
XM_005252591.3:c.861C>A
(CACNB2)
|
XP_005252648.1:p.Tyr287Ter
|
|
|
XM_006717502.3:c.1521C>A
(CACNB2)
|
XP_006717565.1:p.Tyr507Ter
|
|
|
XM_011519659.2:c.1467C>A
(CACNB2)
|
XP_011517961.1:p.Tyr489Ter
|
|
|
XM_017016625.1:c.861C>A
(CACNB2)
|
XP_016872114.1:p.Tyr287Ter
|
|
|
XR_001747060.1:n.2423+2627G>T
(NSUN6)
|
|
|
|
XR_001747198.1:n.1826C>A
(CACNB2)
|
|
|
|
NM_000724.4:c.1536C>A
(CACNB2)
|
NP_000715.2:p.Tyr512Ter
|
|
|
NM_001167945.2:c.1503C>A
(CACNB2)
|
NP_001161417.1:p.Tyr501Ter
|
|
|
NM_001330060.2:c.1422C>A
(CACNB2)
|
NP_001316989.1:p.Tyr474Ter
|
|
|
NM_201570.3:c.1557C>A
(CACNB2)
|
NP_963864.1:p.Tyr519Ter
|
|
|
NM_201571.4:c.1617C>A
(CACNB2)
|
NP_963865.2:p.Tyr539Ter
|
|
|
NM_201572.4:c.1545C>A
(CACNB2)
|
NP_963866.2:p.Tyr515Ter
|
|
|
NM_201590.3:c.1539C>A
(CACNB2)
MANE Plus Clinical
|
NP_963884.2:p.Tyr513Ter
|
|
|
NM_201593.3:c.1587C>A
(CACNB2)
|
NP_963887.2:p.Tyr529Ter
|
|
|
NM_201596.3:c.1701C>A
(CACNB2)
MANE Select
|
NP_963890.2:p.Tyr567Ter
|
|
|
NM_201597.3:c.1629C>A
(CACNB2)
|
NP_963891.1:p.Tyr543Ter
|
|
