ENST00000504915.3:c.5199C>G
|
ENSP00000473355.2:p.Asp1733Glu
|
|
ENST00000505350.2:c.*5151C>G
|
ENSP00000481752.1:n.*5151C>G
|
|
ENST00000507379.6:c.5091C>G
|
ENSP00000423224.2:p.Asp1697Glu
|
|
ENST00000509732.6:c.5145C>G
|
ENSP00000426541.2:p.Asp1715Glu
|
|
ENST00000512211.7:c.5145C>G
|
ENSP00000423828.3:p.Asp1715Glu
|
|
ENST00000257430.9:c.5145C>G
MANE Select
|
ENSP00000257430.4:p.Asp1715Glu
|
|
ENST00000257430.8:c.5145C>G
|
ENSP00000257430.4:p.Asp1715Glu
|
|
ENST00000508376.6:c.5145C>G
|
ENSP00000427089.2:p.Asp1715Glu
|
|
ENST00000508624.5:c.*4467C>G
|
ENSP00000424265.1:n.*4467C>G
|
|
ENST00000520401.1:c.230+11767C>G
|
|
|
NM_000038.5:c.5145C>G
|
NP_000029.2:p.Asp1715Glu
|
|
NM_001127510.2:c.5145C>G
|
NP_001120982.1:p.Asp1715Glu
|
|
NM_001127511.2:c.5091C>G
|
NP_001120983.2:p.Asp1697Glu
|
|
NM_001354895.1:c.5145C>G
|
NP_001341824.1:p.Asp1715Glu
|
|
NM_001354896.1:c.5199C>G
|
NP_001341825.1:p.Asp1733Glu
|
|
NM_001354897.1:c.5175C>G
|
NP_001341826.1:p.Asp1725Glu
|
|
NM_001354898.1:c.5070C>G
|
NP_001341827.1:p.Asp1690Glu
|
|
NM_001354899.1:c.5061C>G
|
NP_001341828.1:p.Asp1687Glu
|
|
NM_001354900.1:c.5022C>G
|
NP_001341829.1:p.Asp1674Glu
|
|
NM_001354901.1:c.4968C>G
|
NP_001341830.1:p.Asp1656Glu
|
|
NM_001354902.1:c.4872C>G
|
NP_001341831.1:p.Asp1624Glu
|
|
NM_001354903.1:c.4842C>G
|
NP_001341832.1:p.Asp1614Glu
|
|
NM_001354904.1:c.4767C>G
|
NP_001341833.1:p.Asp1589Glu
|
|
NM_001354905.1:c.4665C>G
|
NP_001341834.1:p.Asp1555Glu
|
|
NM_001354906.1:c.4296C>G
|
NP_001341835.1:p.Asp1432Glu
|
|
NM_000038.6:c.5145C>G
MANE Select
|
NP_000029.2:p.Asp1715Glu
|
|
NM_001127510.3:c.5145C>G
|
NP_001120982.1:p.Asp1715Glu
|
|
NM_001127511.3:c.5091C>G
|
NP_001120983.2:p.Asp1697Glu
|
|
NM_001354895.2:c.5145C>G
|
NP_001341824.1:p.Asp1715Glu
|
|
NM_001354896.2:c.5199C>G
|
NP_001341825.1:p.Asp1733Glu
|
|
NM_001354897.2:c.5175C>G
|
NP_001341826.1:p.Asp1725Glu
|
|
NM_001354898.2:c.5070C>G
|
NP_001341827.1:p.Asp1690Glu
|
|
NM_001354899.2:c.5061C>G
|
NP_001341828.1:p.Asp1687Glu
|
|
NM_001354900.2:c.5022C>G
|
NP_001341829.1:p.Asp1674Glu
|
|
NM_001354901.2:c.4968C>G
|
NP_001341830.1:p.Asp1656Glu
|
|
NM_001354902.2:c.4872C>G
|
NP_001341831.1:p.Asp1624Glu
|
|
NM_001354903.2:c.4842C>G
|
NP_001341832.1:p.Asp1614Glu
|
|
NM_001354904.2:c.4767C>G
|
NP_001341833.1:p.Asp1589Glu
|
|
NM_001354905.2:c.4665C>G
|
NP_001341834.1:p.Asp1555Glu
|
|
NM_001354906.2:c.4296C>G
|
NP_001341835.1:p.Asp1432Glu
|
|