ENST00000504915.3:c.8199C>A
|
ENSP00000473355.2:p.Thr2733=
|
|
ENST00000505350.2:c.*8151C>A
|
ENSP00000481752.1:n.*8151C>A
|
|
ENST00000507379.6:c.8091C>A
|
ENSP00000423224.2:p.Thr2697=
|
|
ENST00000509732.6:c.8145C>A
|
ENSP00000426541.2:p.Thr2715=
|
|
ENST00000512211.7:c.8145C>A
|
ENSP00000423828.3:p.Thr2715=
|
|
ENST00000257430.9:c.8145C>A
MANE Select
|
ENSP00000257430.4:p.Thr2715=
|
|
ENST00000257430.8:c.8145C>A
|
ENSP00000257430.4:p.Thr2715=
|
|
ENST00000508376.6:c.8145C>A
|
ENSP00000427089.2:p.Thr2715=
|
|
ENST00000520401.1:c.231-12910C>A
|
|
|
NM_000038.5:c.8145C>A
|
NP_000029.2:p.Thr2715=
|
|
NM_001127510.2:c.8145C>A
|
NP_001120982.1:p.Thr2715=
|
|
NM_001127511.2:c.8091C>A
|
NP_001120983.2:p.Thr2697=
|
|
NM_001354895.1:c.8145C>A
|
NP_001341824.1:p.Thr2715=
|
|
NM_001354896.1:c.8199C>A
|
NP_001341825.1:p.Thr2733=
|
|
NM_001354897.1:c.8175C>A
|
NP_001341826.1:p.Thr2725=
|
|
NM_001354898.1:c.8070C>A
|
NP_001341827.1:p.Thr2690=
|
|
NM_001354899.1:c.8061C>A
|
NP_001341828.1:p.Thr2687=
|
|
NM_001354900.1:c.8022C>A
|
NP_001341829.1:p.Thr2674=
|
|
NM_001354901.1:c.7968C>A
|
NP_001341830.1:p.Thr2656=
|
|
NM_001354902.1:c.7872C>A
|
NP_001341831.1:p.Thr2624=
|
|
NM_001354903.1:c.7842C>A
|
NP_001341832.1:p.Thr2614=
|
|
NM_001354904.1:c.7767C>A
|
NP_001341833.1:p.Thr2589=
|
|
NM_001354905.1:c.7665C>A
|
NP_001341834.1:p.Thr2555=
|
|
NM_001354906.1:c.7296C>A
|
NP_001341835.1:p.Thr2432=
|
|
NM_000038.6:c.8145C>A
MANE Select
|
NP_000029.2:p.Thr2715=
|
|
NM_001127510.3:c.8145C>A
|
NP_001120982.1:p.Thr2715=
|
|
NM_001127511.3:c.8091C>A
|
NP_001120983.2:p.Thr2697=
|
|
NM_001354895.2:c.8145C>A
|
NP_001341824.1:p.Thr2715=
|
|
NM_001354896.2:c.8199C>A
|
NP_001341825.1:p.Thr2733=
|
|
NM_001354897.2:c.8175C>A
|
NP_001341826.1:p.Thr2725=
|
|
NM_001354898.2:c.8070C>A
|
NP_001341827.1:p.Thr2690=
|
|
NM_001354899.2:c.8061C>A
|
NP_001341828.1:p.Thr2687=
|
|
NM_001354900.2:c.8022C>A
|
NP_001341829.1:p.Thr2674=
|
|
NM_001354901.2:c.7968C>A
|
NP_001341830.1:p.Thr2656=
|
|
NM_001354902.2:c.7872C>A
|
NP_001341831.1:p.Thr2624=
|
|
NM_001354903.2:c.7842C>A
|
NP_001341832.1:p.Thr2614=
|
|
NM_001354904.2:c.7767C>A
|
NP_001341833.1:p.Thr2589=
|
|
NM_001354905.2:c.7665C>A
|
NP_001341834.1:p.Thr2555=
|
|
NM_001354906.2:c.7296C>A
|
NP_001341835.1:p.Thr2432=
|
|