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NM_000038.6:c.3469G>T
MANE Select
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NP_000029.2:p.Glu1157Ter
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ENST00000257430.9:c.3469G>T
MANE Select
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ENSP00000257430.4:p.Glu1157Ter
|
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NM_000038.5:c.3469G>T
|
NP_000029.2:p.Glu1157Ter
|
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NM_001127510.2:c.3469G>T
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NP_001120982.1:p.Glu1157Ter
|
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NM_001127510.3:c.3469G>T
|
NP_001120982.1:p.Glu1157Ter
|
|
NM_001127511.2:c.3415G>T
|
NP_001120983.2:p.Glu1139Ter
|
|
NM_001127511.3:c.3415G>T
|
NP_001120983.2:p.Glu1139Ter
|
|
NM_001354895.1:c.3469G>T
|
NP_001341824.1:p.Glu1157Ter
|
|
NM_001354895.2:c.3469G>T
|
NP_001341824.1:p.Glu1157Ter
|
|
NM_001354896.1:c.3523G>T
|
NP_001341825.1:p.Glu1175Ter
|
|
NM_001354896.2:c.3523G>T
|
NP_001341825.1:p.Glu1175Ter
|
|
NM_001354897.1:c.3499G>T
|
NP_001341826.1:p.Glu1167Ter
|
|
NM_001354897.2:c.3499G>T
|
NP_001341826.1:p.Glu1167Ter
|
|
NM_001354898.1:c.3394G>T
|
NP_001341827.1:p.Glu1132Ter
|
|
NM_001354898.2:c.3394G>T
|
NP_001341827.1:p.Glu1132Ter
|
|
NM_001354899.1:c.3385G>T
|
NP_001341828.1:p.Glu1129Ter
|
|
NM_001354899.2:c.3385G>T
|
NP_001341828.1:p.Glu1129Ter
|
|
NM_001354900.1:c.3346G>T
|
NP_001341829.1:p.Glu1116Ter
|
|
NM_001354900.2:c.3346G>T
|
NP_001341829.1:p.Glu1116Ter
|
|
NM_001354901.1:c.3292G>T
|
NP_001341830.1:p.Glu1098Ter
|
|
NM_001354901.2:c.3292G>T
|
NP_001341830.1:p.Glu1098Ter
|
|
NM_001354902.1:c.3196G>T
|
NP_001341831.1:p.Glu1066Ter
|
|
NM_001354902.2:c.3196G>T
|
NP_001341831.1:p.Glu1066Ter
|
|
NM_001354903.1:c.3166G>T
|
NP_001341832.1:p.Glu1056Ter
|
|
NM_001354903.2:c.3166G>T
|
NP_001341832.1:p.Glu1056Ter
|
|
NM_001354904.1:c.3091G>T
|
NP_001341833.1:p.Glu1031Ter
|
|
NM_001354904.2:c.3091G>T
|
NP_001341833.1:p.Glu1031Ter
|
|
NM_001354905.1:c.2989G>T
|
NP_001341834.1:p.Glu997Ter
|
|
NM_001354905.2:c.2989G>T
|
NP_001341834.1:p.Glu997Ter
|
|
NM_001354906.1:c.2620G>T
|
NP_001341835.1:p.Glu874Ter
|
|
NM_001354906.2:c.2620G>T
|
NP_001341835.1:p.Glu874Ter
|
|
ENST00000257430.8:c.3469G>T
|
ENSP00000257430.4:p.Glu1157Ter
|
|
ENST00000502371.2:c.1822G>T
|
|
|
ENST00000502371.3:c.3134G>T
|
ENSP00000484935.2:n.3134G>T
|
|
ENST00000504915.3:c.3523G>T
|
ENSP00000473355.2:p.Glu1175Ter
|
|
ENST00000505350.2:c.*3475G>T
|
ENSP00000481752.1:n.*3475G>T
|
|
ENST00000507379.6:c.3415G>T
|
ENSP00000423224.2:p.Glu1139Ter
|
|
ENST00000508376.6:c.3469G>T
|
ENSP00000427089.2:p.Glu1157Ter
|
|
ENST00000508624.5:c.*2791G>T
|
ENSP00000424265.1:n.*2791G>T
|
|
ENST00000509732.6:c.3469G>T
|
ENSP00000426541.2:p.Glu1157Ter
|
|
ENST00000512211.6:c.3469G>T
|
ENSP00000423828.2:p.Glu1157Ter
|
|
ENST00000512211.7:c.3469G>T
|
ENSP00000423828.3:p.Glu1157Ter
|
|
ENST00000520401.1:c.230+10091G>T
|
|