ENST00000502371.3:c.3685T>C
|
ENSP00000484935.2:n.3685T>C
|
|
ENST00000504915.3:c.4074T>C
|
ENSP00000473355.2:p.Ser1358=
|
|
ENST00000505350.2:c.*4026T>C
|
ENSP00000481752.1:n.*4026T>C
|
|
ENST00000507379.6:c.3966T>C
|
ENSP00000423224.2:p.Ser1322=
|
|
ENST00000509732.6:c.4020T>C
|
ENSP00000426541.2:p.Ser1340=
|
|
ENST00000512211.7:c.4020T>C
|
ENSP00000423828.3:p.Ser1340=
|
|
ENST00000257430.9:c.4020T>C
MANE Select
|
ENSP00000257430.4:p.Ser1340=
|
|
ENST00000257430.8:c.4020T>C
|
ENSP00000257430.4:p.Ser1340=
|
|
ENST00000502371.2:c.2373T>C
|
|
|
ENST00000508376.6:c.4020T>C
|
ENSP00000427089.2:p.Ser1340=
|
|
ENST00000508624.5:c.*3342T>C
|
ENSP00000424265.1:n.*3342T>C
|
|
ENST00000520401.1:c.230+10642T>C
|
|
|
NM_000038.5:c.4020T>C
|
NP_000029.2:p.Ser1340=
|
|
NM_001127510.2:c.4020T>C
|
NP_001120982.1:p.Ser1340=
|
|
NM_001127511.2:c.3966T>C
|
NP_001120983.2:p.Ser1322=
|
|
NM_001354895.1:c.4020T>C
|
NP_001341824.1:p.Ser1340=
|
|
NM_001354896.1:c.4074T>C
|
NP_001341825.1:p.Ser1358=
|
|
NM_001354897.1:c.4050T>C
|
NP_001341826.1:p.Ser1350=
|
|
NM_001354898.1:c.3945T>C
|
NP_001341827.1:p.Ser1315=
|
|
NM_001354899.1:c.3936T>C
|
NP_001341828.1:p.Ser1312=
|
|
NM_001354900.1:c.3897T>C
|
NP_001341829.1:p.Ser1299=
|
|
NM_001354901.1:c.3843T>C
|
NP_001341830.1:p.Ser1281=
|
|
NM_001354902.1:c.3747T>C
|
NP_001341831.1:p.Ser1249=
|
|
NM_001354903.1:c.3717T>C
|
NP_001341832.1:p.Ser1239=
|
|
NM_001354904.1:c.3642T>C
|
NP_001341833.1:p.Ser1214=
|
|
NM_001354905.1:c.3540T>C
|
NP_001341834.1:p.Ser1180=
|
|
NM_001354906.1:c.3171T>C
|
NP_001341835.1:p.Ser1057=
|
|
NM_000038.6:c.4020T>C
MANE Select
|
NP_000029.2:p.Ser1340=
|
|
NM_001127510.3:c.4020T>C
|
NP_001120982.1:p.Ser1340=
|
|
NM_001127511.3:c.3966T>C
|
NP_001120983.2:p.Ser1322=
|
|
NM_001354895.2:c.4020T>C
|
NP_001341824.1:p.Ser1340=
|
|
NM_001354896.2:c.4074T>C
|
NP_001341825.1:p.Ser1358=
|
|
NM_001354897.2:c.4050T>C
|
NP_001341826.1:p.Ser1350=
|
|
NM_001354898.2:c.3945T>C
|
NP_001341827.1:p.Ser1315=
|
|
NM_001354899.2:c.3936T>C
|
NP_001341828.1:p.Ser1312=
|
|
NM_001354900.2:c.3897T>C
|
NP_001341829.1:p.Ser1299=
|
|
NM_001354901.2:c.3843T>C
|
NP_001341830.1:p.Ser1281=
|
|
NM_001354902.2:c.3747T>C
|
NP_001341831.1:p.Ser1249=
|
|
NM_001354903.2:c.3717T>C
|
NP_001341832.1:p.Ser1239=
|
|
NM_001354904.2:c.3642T>C
|
NP_001341833.1:p.Ser1214=
|
|
NM_001354905.2:c.3540T>C
|
NP_001341834.1:p.Ser1180=
|
|
NM_001354906.2:c.3171T>C
|
NP_001341835.1:p.Ser1057=
|
|