|
NM_000038.6:c.5562C>G
MANE Select
|
NP_000029.2:p.Tyr1854Ter
|
|
ENST00000257430.9:c.5562C>G
MANE Select
|
ENSP00000257430.4:p.Tyr1854Ter
|
|
NM_000038.5:c.5562C>G
|
NP_000029.2:p.Tyr1854Ter
|
|
NM_001127510.2:c.5562C>G
|
NP_001120982.1:p.Tyr1854Ter
|
|
NM_001127510.3:c.5562C>G
|
NP_001120982.1:p.Tyr1854Ter
|
|
NM_001127511.2:c.5508C>G
|
NP_001120983.2:p.Tyr1836Ter
|
|
NM_001127511.3:c.5508C>G
|
NP_001120983.2:p.Tyr1836Ter
|
|
NM_001354895.1:c.5562C>G
|
NP_001341824.1:p.Tyr1854Ter
|
|
NM_001354895.2:c.5562C>G
|
NP_001341824.1:p.Tyr1854Ter
|
|
NM_001354896.1:c.5616C>G
|
NP_001341825.1:p.Tyr1872Ter
|
|
NM_001354896.2:c.5616C>G
|
NP_001341825.1:p.Tyr1872Ter
|
|
NM_001354897.1:c.5592C>G
|
NP_001341826.1:p.Tyr1864Ter
|
|
NM_001354897.2:c.5592C>G
|
NP_001341826.1:p.Tyr1864Ter
|
|
NM_001354898.1:c.5487C>G
|
NP_001341827.1:p.Tyr1829Ter
|
|
NM_001354898.2:c.5487C>G
|
NP_001341827.1:p.Tyr1829Ter
|
|
NM_001354899.1:c.5478C>G
|
NP_001341828.1:p.Tyr1826Ter
|
|
NM_001354899.2:c.5478C>G
|
NP_001341828.1:p.Tyr1826Ter
|
|
NM_001354900.1:c.5439C>G
|
NP_001341829.1:p.Tyr1813Ter
|
|
NM_001354900.2:c.5439C>G
|
NP_001341829.1:p.Tyr1813Ter
|
|
NM_001354901.1:c.5385C>G
|
NP_001341830.1:p.Tyr1795Ter
|
|
NM_001354901.2:c.5385C>G
|
NP_001341830.1:p.Tyr1795Ter
|
|
NM_001354902.1:c.5289C>G
|
NP_001341831.1:p.Tyr1763Ter
|
|
NM_001354902.2:c.5289C>G
|
NP_001341831.1:p.Tyr1763Ter
|
|
NM_001354903.1:c.5259C>G
|
NP_001341832.1:p.Tyr1753Ter
|
|
NM_001354903.2:c.5259C>G
|
NP_001341832.1:p.Tyr1753Ter
|
|
NM_001354904.1:c.5184C>G
|
NP_001341833.1:p.Tyr1728Ter
|
|
NM_001354904.2:c.5184C>G
|
NP_001341833.1:p.Tyr1728Ter
|
|
NM_001354905.1:c.5082C>G
|
NP_001341834.1:p.Tyr1694Ter
|
|
NM_001354905.2:c.5082C>G
|
NP_001341834.1:p.Tyr1694Ter
|
|
NM_001354906.1:c.4713C>G
|
NP_001341835.1:p.Tyr1571Ter
|
|
NM_001354906.2:c.4713C>G
|
NP_001341835.1:p.Tyr1571Ter
|
|
ENST00000257430.8:c.5562C>G
|
ENSP00000257430.4:p.Tyr1854Ter
|
|
ENST00000504915.3:c.5616C>G
|
ENSP00000473355.2:p.Tyr1872Ter
|
|
ENST00000505350.2:c.*5568C>G
|
ENSP00000481752.1:n.*5568C>G
|
|
ENST00000507379.6:c.5508C>G
|
ENSP00000423224.2:p.Tyr1836Ter
|
|
ENST00000508376.6:c.5562C>G
|
ENSP00000427089.2:p.Tyr1854Ter
|
|
ENST00000508624.5:c.*4884C>G
|
ENSP00000424265.1:n.*4884C>G
|
|
ENST00000509732.6:c.5562C>G
|
ENSP00000426541.2:p.Tyr1854Ter
|
|
ENST00000512211.7:c.5562C>G
|
ENSP00000423828.3:p.Tyr1854Ter
|
|
ENST00000520401.1:c.230+12184C>G
|
|