|
NM_000038.6:c.8446C>T
MANE Select
|
NP_000029.2:p.Arg2816Ter
|
|
ENST00000257430.9:c.8446C>T
MANE Select
|
ENSP00000257430.4:p.Arg2816Ter
|
|
NM_000038.5:c.8446C>T
|
NP_000029.2:p.Arg2816Ter
|
|
NM_001127510.2:c.8446C>T
|
NP_001120982.1:p.Arg2816Ter
|
|
NM_001127510.3:c.8446C>T
|
NP_001120982.1:p.Arg2816Ter
|
|
NM_001127511.2:c.8392C>T
|
NP_001120983.2:p.Arg2798Ter
|
|
NM_001127511.3:c.8392C>T
|
NP_001120983.2:p.Arg2798Ter
|
|
NM_001354895.1:c.8446C>T
|
NP_001341824.1:p.Arg2816Ter
|
|
NM_001354895.2:c.8446C>T
|
NP_001341824.1:p.Arg2816Ter
|
|
NM_001354896.1:c.8500C>T
|
NP_001341825.1:p.Arg2834Ter
|
|
NM_001354896.2:c.8500C>T
|
NP_001341825.1:p.Arg2834Ter
|
|
NM_001354897.1:c.8476C>T
|
NP_001341826.1:p.Arg2826Ter
|
|
NM_001354897.2:c.8476C>T
|
NP_001341826.1:p.Arg2826Ter
|
|
NM_001354898.1:c.8371C>T
|
NP_001341827.1:p.Arg2791Ter
|
|
NM_001354898.2:c.8371C>T
|
NP_001341827.1:p.Arg2791Ter
|
|
NM_001354899.1:c.8362C>T
|
NP_001341828.1:p.Arg2788Ter
|
|
NM_001354899.2:c.8362C>T
|
NP_001341828.1:p.Arg2788Ter
|
|
NM_001354900.1:c.8323C>T
|
NP_001341829.1:p.Arg2775Ter
|
|
NM_001354900.2:c.8323C>T
|
NP_001341829.1:p.Arg2775Ter
|
|
NM_001354901.1:c.8269C>T
|
NP_001341830.1:p.Arg2757Ter
|
|
NM_001354901.2:c.8269C>T
|
NP_001341830.1:p.Arg2757Ter
|
|
NM_001354902.1:c.8173C>T
|
NP_001341831.1:p.Arg2725Ter
|
|
NM_001354902.2:c.8173C>T
|
NP_001341831.1:p.Arg2725Ter
|
|
NM_001354903.1:c.8143C>T
|
NP_001341832.1:p.Arg2715Ter
|
|
NM_001354903.2:c.8143C>T
|
NP_001341832.1:p.Arg2715Ter
|
|
NM_001354904.1:c.8068C>T
|
NP_001341833.1:p.Arg2690Ter
|
|
NM_001354904.2:c.8068C>T
|
NP_001341833.1:p.Arg2690Ter
|
|
NM_001354905.1:c.7966C>T
|
NP_001341834.1:p.Arg2656Ter
|
|
NM_001354905.2:c.7966C>T
|
NP_001341834.1:p.Arg2656Ter
|
|
NM_001354906.1:c.7597C>T
|
NP_001341835.1:p.Arg2533Ter
|
|
NM_001354906.2:c.7597C>T
|
NP_001341835.1:p.Arg2533Ter
|
|
ENST00000257430.8:c.8446C>T
|
ENSP00000257430.4:p.Arg2816Ter
|
|
ENST00000504915.3:c.8500C>T
|
ENSP00000473355.2:p.Arg2834Ter
|
|
ENST00000505350.2:c.*8452C>T
|
ENSP00000481752.1:n.*8452C>T
|
|
ENST00000507379.6:c.8392C>T
|
ENSP00000423224.2:p.Arg2798Ter
|
|
ENST00000508376.6:c.8446C>T
|
ENSP00000427089.2:p.Arg2816Ter
|
|
ENST00000509732.6:c.8446C>T
|
ENSP00000426541.2:p.Arg2816Ter
|
|
ENST00000512211.7:c.8446C>T
|
ENSP00000423828.3:p.Arg2816Ter
|
|
ENST00000520401.1:c.231-12609C>T
|
|
