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NM_000038.6:c.3856G>T
MANE Select
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NP_000029.2:p.Glu1286Ter
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ENST00000257430.9:c.3856G>T
MANE Select
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ENSP00000257430.4:p.Glu1286Ter
|
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NM_000038.5:c.3856G>T
|
NP_000029.2:p.Glu1286Ter
|
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NM_001127510.2:c.3856G>T
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NP_001120982.1:p.Glu1286Ter
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NM_001127510.3:c.3856G>T
|
NP_001120982.1:p.Glu1286Ter
|
|
NM_001127511.2:c.3802G>T
|
NP_001120983.2:p.Glu1268Ter
|
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NM_001127511.3:c.3802G>T
|
NP_001120983.2:p.Glu1268Ter
|
|
NM_001354895.1:c.3856G>T
|
NP_001341824.1:p.Glu1286Ter
|
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NM_001354895.2:c.3856G>T
|
NP_001341824.1:p.Glu1286Ter
|
|
NM_001354896.1:c.3910G>T
|
NP_001341825.1:p.Glu1304Ter
|
|
NM_001354896.2:c.3910G>T
|
NP_001341825.1:p.Glu1304Ter
|
|
NM_001354897.1:c.3886G>T
|
NP_001341826.1:p.Glu1296Ter
|
|
NM_001354897.2:c.3886G>T
|
NP_001341826.1:p.Glu1296Ter
|
|
NM_001354898.1:c.3781G>T
|
NP_001341827.1:p.Glu1261Ter
|
|
NM_001354898.2:c.3781G>T
|
NP_001341827.1:p.Glu1261Ter
|
|
NM_001354899.1:c.3772G>T
|
NP_001341828.1:p.Glu1258Ter
|
|
NM_001354899.2:c.3772G>T
|
NP_001341828.1:p.Glu1258Ter
|
|
NM_001354900.1:c.3733G>T
|
NP_001341829.1:p.Glu1245Ter
|
|
NM_001354900.2:c.3733G>T
|
NP_001341829.1:p.Glu1245Ter
|
|
NM_001354901.1:c.3679G>T
|
NP_001341830.1:p.Glu1227Ter
|
|
NM_001354901.2:c.3679G>T
|
NP_001341830.1:p.Glu1227Ter
|
|
NM_001354902.1:c.3583G>T
|
NP_001341831.1:p.Glu1195Ter
|
|
NM_001354902.2:c.3583G>T
|
NP_001341831.1:p.Glu1195Ter
|
|
NM_001354903.1:c.3553G>T
|
NP_001341832.1:p.Glu1185Ter
|
|
NM_001354903.2:c.3553G>T
|
NP_001341832.1:p.Glu1185Ter
|
|
NM_001354904.1:c.3478G>T
|
NP_001341833.1:p.Glu1160Ter
|
|
NM_001354904.2:c.3478G>T
|
NP_001341833.1:p.Glu1160Ter
|
|
NM_001354905.1:c.3376G>T
|
NP_001341834.1:p.Glu1126Ter
|
|
NM_001354905.2:c.3376G>T
|
NP_001341834.1:p.Glu1126Ter
|
|
NM_001354906.1:c.3007G>T
|
NP_001341835.1:p.Glu1003Ter
|
|
NM_001354906.2:c.3007G>T
|
NP_001341835.1:p.Glu1003Ter
|
|
ENST00000257430.8:c.3856G>T
|
ENSP00000257430.4:p.Glu1286Ter
|
|
ENST00000502371.2:c.2209G>T
|
|
|
ENST00000502371.3:c.3521G>T
|
ENSP00000484935.2:n.3521G>T
|
|
ENST00000504915.3:c.3910G>T
|
ENSP00000473355.2:p.Glu1304Ter
|
|
ENST00000505350.2:c.*3862G>T
|
ENSP00000481752.1:n.*3862G>T
|
|
ENST00000507379.6:c.3802G>T
|
ENSP00000423224.2:p.Glu1268Ter
|
|
ENST00000508376.6:c.3856G>T
|
ENSP00000427089.2:p.Glu1286Ter
|
|
ENST00000508624.5:c.*3178G>T
|
ENSP00000424265.1:n.*3178G>T
|
|
ENST00000509732.6:c.3856G>T
|
ENSP00000426541.2:p.Glu1286Ter
|
|
ENST00000512211.6:c.3856G>T
|
ENSP00000423828.2:p.Glu1286Ter
|
|
ENST00000512211.7:c.3856G>T
|
ENSP00000423828.3:p.Glu1286Ter
|
|
ENST00000520401.1:c.230+10478G>T
|
|