|
ENST00000377315.6:c.729G>A
(CACNB2)
|
ENSP00000366532.4:p.Leu243=
|
|
|
ENST00000377319.9:c.594G>A
(CACNB2)
|
ENSP00000366536.3:p.Leu198=
|
|
|
ENST00000645287.2:c.717G>A
(CACNB2)
|
ENSP00000496203.1:p.Leu239=
|
|
|
ENST00000282343.13:c.789G>A
(CACNB2)
|
ENSP00000282343.8:p.Leu263=
|
|
|
ENST00000324631.13:c.873G>A
(CACNB2)
MANE Select
|
ENSP00000320025.8:p.Leu291=
|
|
|
ENST00000377315.5:c.729G>A
(CACNB2)
|
ENSP00000366532.4:p.Leu243=
|
|
|
ENST00000377319.8:c.594G>A
(CACNB2)
|
ENSP00000366536.3:p.Leu198=
|
|
|
ENST00000377329.10:c.711G>A
(CACNB2)
MANE Plus Clinical
|
ENSP00000366546.4:p.Leu237=
|
|
|
ENST00000377331.8:c.594G>A
(CACNB2)
|
ENSP00000366548.4:p.Leu198=
|
|
|
ENST00000643096.2:c.675G>A
(CACNB2)
|
ENSP00000494209.2:p.Leu225=
|
|
|
ENST00000643330.1:n.960G>A
(CACNB2)
|
|
|
|
ENST00000644004.1:c.*14G>A
(CACNB2)
|
ENSP00000495509.1:n.*14G>A
|
|
|
ENST00000645287.1:c.717G>A
(CACNB2)
|
ENSP00000496203.1:p.Leu239=
|
|
|
ENST00000647168.2:c.*14G>A
(CACNB2)
|
ENSP00000495854.2:n.*14G>A
|
|
|
ENST00000650685.1:c.615G>A
(CACNB2)
|
ENSP00000498460.1:p.Leu205=
|
|
|
ENST00000651330.1:c.*147G>A
(CACNB2)
|
ENSP00000498457.1:n.*147G>A
|
|
|
ENST00000651468.1:c.430G>A
(CACNB2)
|
ENSP00000498352.1:n.430G>A
|
|
|
ENST00000651928.1:c.*112G>A
(CACNB2)
|
ENSP00000499177.1:n.*112G>A
|
|
|
ENST00000652391.1:c.693G>A
(CACNB2)
|
ENSP00000498938.1:p.Leu231=
|
|
|
ENST00000652478.1:c.729G>A
(CACNB2)
|
ENSP00000498812.1:p.Leu243=
|
|
|
ENST00000282343.12:c.789G>A
(CACNB2)
|
ENSP00000282343.8:p.Leu263=
|
|
|
ENST00000324631.11:c.873G>A
(CACNB2)
|
ENSP00000320025.7:p.Leu291=
|
|
|
ENST00000352115.10:c.801G>A
(CACNB2)
|
ENSP00000344474.6:p.Leu267=
|
|
|
ENST00000377315.4:c.729G>A
(CACNB2)
|
ENSP00000366532.4:p.Leu243=
|
|
|
ENST00000377319.7:c.594G>A
(CACNB2)
|
ENSP00000366536.3:p.Leu198=
|
|
|
ENST00000377328.5:c.457-17697G>A
(CACNB2)
|
ENSP00000366545.1:n.457-17697G>A
|
|
|
ENST00000377329.8:c.711G>A
(CACNB2)
|
ENSP00000366546.4:p.Leu237=
|
|
|
ENST00000377331.6:c.717G>A
(CACNB2)
|
ENSP00000366548.2:p.Leu239=
|
|
|
ENST00000396576.6:c.708G>A
(CACNB2)
|
ENSP00000379821.2:p.Leu236=
|
|
|
ENST00000612134.4:c.577G>A
(CACNB2)
|
ENSP00000480563.1:n.577G>A
|
|
|
ENST00000612743.1:c.35-20860G>A
(CACNB2)
|
ENSP00000478676.1:n.35-20860G>A
|
|
|
ENST00000615785.4:c.292-17697G>A
(CACNB2)
|
ENSP00000480260.1:n.292-17697G>A
|
|
|
ENST00000617363.4:c.636G>A
(CACNB2)
|
ENSP00000479756.1:p.Leu212=
|
|
|
NM_000724.3:c.708G>A
(CACNB2)
|
NP_000715.2:p.Leu236=
|
|
|
NM_001167945.1:c.675G>A
(CACNB2)
|
NP_001161417.1:p.Leu225=
|
|
|
NM_201570.2:c.729G>A
(CACNB2)
|
NP_963864.1:p.Leu243=
|
|
|
NM_201571.3:c.789G>A
(CACNB2)
|
NP_963865.2:p.Leu263=
|
|
|
NM_201572.3:c.717G>A
(CACNB2)
|
NP_963866.2:p.Leu239=
|
|
|
NM_201590.2:c.711G>A
(CACNB2)
|
NP_963884.2:p.Leu237=
|
|
|
NM_201593.2:c.759G>A
(CACNB2)
|
NP_963887.2:p.Leu253=
|
|
|
NM_201596.2:c.873G>A
(CACNB2)
|
NP_963890.2:p.Leu291=
|
|
|
NM_201597.2:c.801G>A
(CACNB2)
|
NP_963891.1:p.Leu267=
|
|
|
XM_005252588.2:c.615G>A
(CACNB2)
|
XP_005252645.1:p.Leu205=
|
|
|
XM_005252591.2:c.33G>A
(CACNB2)
|
XP_005252648.1:p.Leu11=
|
|
|
XM_006717502.2:c.693G>A
(CACNB2)
|
XP_006717565.1:p.Leu231=
|
|
|
XM_011519659.1:c.639G>A
(CACNB2)
|
XP_011517961.1:p.Leu213=
|
|
|
XM_011519660.1:c.594G>A
(CACNB2)
|
XP_011517962.1:p.Leu198=
|
|
|
XR_930717.1:n.73-4744C>T
|
|
|
|
XR_930718.1:n.1034-4744C>T
|
|
|
|
NM_001330060.1:c.594G>A
(CACNB2)
|
NP_001316989.1:p.Leu198=
|
|
|
XM_005252588.4:c.615G>A
(CACNB2)
|
XP_005252645.1:p.Leu205=
|
|
|
XM_005252591.3:c.33G>A
(CACNB2)
|
XP_005252648.1:p.Leu11=
|
|
|
XM_006717502.3:c.693G>A
(CACNB2)
|
XP_006717565.1:p.Leu231=
|
|
|
XM_011519659.2:c.639G>A
(CACNB2)
|
XP_011517961.1:p.Leu213=
|
|
|
XM_017016625.1:c.33G>A
(CACNB2)
|
XP_016872114.1:p.Leu11=
|
|
|
XR_001747060.1:n.2424-4744C>T
(NSUN6)
|
|
|
|
XR_001747198.1:n.998G>A
(CACNB2)
|
|
|
|
NM_000724.4:c.708G>A
(CACNB2)
|
NP_000715.2:p.Leu236=
|
|
|
NM_001167945.2:c.675G>A
(CACNB2)
|
NP_001161417.1:p.Leu225=
|
|
|
NM_001330060.2:c.594G>A
(CACNB2)
|
NP_001316989.1:p.Leu198=
|
|
|
NM_201570.3:c.729G>A
(CACNB2)
|
NP_963864.1:p.Leu243=
|
|
|
NM_201571.4:c.789G>A
(CACNB2)
|
NP_963865.2:p.Leu263=
|
|
|
NM_201572.4:c.717G>A
(CACNB2)
|
NP_963866.2:p.Leu239=
|
|
|
NM_201590.3:c.711G>A
(CACNB2)
MANE Plus Clinical
|
NP_963884.2:p.Leu237=
|
|
|
NM_201593.3:c.759G>A
(CACNB2)
|
NP_963887.2:p.Leu253=
|
|
|
NM_201596.3:c.873G>A
(CACNB2)
MANE Select
|
NP_963890.2:p.Leu291=
|
|
|
NM_201597.3:c.801G>A
(CACNB2)
|
NP_963891.1:p.Leu267=
|
|
