ENST00000524561.2:n.3057T>C
|
|
|
ENST00000528374.2:c.67T>C
|
|
|
ENST00000529967.6:n.1827T>C
|
|
|
ENST00000532220.2:n.1220T>C
|
|
|
ENST00000642611.2:n.3557T>C
|
|
|
ENST00000645004.2:n.987T>C
|
|
|
ENST00000682051.1:n.3504T>C
|
|
|
ENST00000682110.1:n.3557T>C
|
|
|
ENST00000682140.1:c.3485T>C
|
ENSP00000507829.1:p.Phe1162Ser
|
|
ENST00000682185.1:n.4793T>C
|
|
|
ENST00000682204.1:c.*1626T>C
|
ENSP00000507094.1:n.*1626T>C
|
|
ENST00000682215.1:n.3554T>C
|
|
|
ENST00000682288.1:c.*1919T>C
|
ENSP00000507506.1:n.*1919T>C
|
|
ENST00000682442.1:n.3777T>C
|
|
|
ENST00000682528.1:n.3634T>C
|
|
|
ENST00000682673.1:n.3501T>C
|
|
|
ENST00000682805.1:n.3554T>C
|
|
|
ENST00000682965.1:c.3396+913T>C
|
ENSP00000508229.1:n.3396+913T>C
|
|
ENST00000683093.1:n.3656T>C
|
|
|
ENST00000683136.1:c.3485T>C
|
ENSP00000507768.1:p.Phe1162Ser
|
|
ENST00000683153.1:n.3713T>C
|
|
|
ENST00000683365.1:n.3659T>C
|
|
|
ENST00000683377.1:n.3557T>C
|
|
|
ENST00000683456.1:c.*625T>C
|
ENSP00000508318.1:n.*625T>C
|
|
ENST00000683522.1:n.3557T>C
|
|
|
ENST00000683562.1:c.*1657T>C
|
ENSP00000508265.1:n.*1657T>C
|
|
ENST00000683693.1:n.3634T>C
|
|
|
ENST00000683725.1:c.3488T>C
|
ENSP00000507496.1:p.Phe1163Ser
|
|
ENST00000684010.1:n.3552T>C
|
|
|
ENST00000684157.1:n.3557T>C
|
|
|
ENST00000684253.1:n.3460T>C
|
|
|
ENST00000684288.1:c.*1660T>C
|
ENSP00000507143.1:n.*1660T>C
|
|
ENST00000684313.1:n.2989T>C
|
|
|
ENST00000684332.1:n.3630T>C
|
|
|
ENST00000684371.1:n.3663T>C
|
|
|
ENST00000684404.1:n.3600T>C
|
|
|
ENST00000684442.1:n.3557T>C
|
|
|
ENST00000684555.1:c.*1700T>C
|
ENSP00000507705.1:n.*1700T>C
|
|
ENST00000684571.1:c.3329T>C
|
ENSP00000506935.1:p.Phe1110Ser
|
|
ENST00000684593.1:c.*3193T>C
|
ENSP00000507005.1:n.*3193T>C
|
|
ENST00000684711.1:c.*1884T>C
|
ENSP00000506841.1:n.*1884T>C
|
|
ENST00000302539.9:c.3491T>C
|
ENSP00000303960.4:p.Phe1164Ser
|
|
ENST00000389817.8:c.3488T>C
MANE Select
|
ENSP00000374467.4:p.Phe1163Ser
|
|
ENST00000642271.1:c.3485T>C
|
ENSP00000493749.1:p.Phe1162Ser
|
|
ENST00000642579.1:c.1572T>C
|
|
|
ENST00000642611.1:n.3442T>C
|
|
|
ENST00000642902.1:c.3270T>C
|
|
|
ENST00000643260.1:c.3488T>C
|
ENSP00000494450.1:p.Phe1163Ser
|
|
ENST00000643562.1:c.*1464T>C
|
ENSP00000496124.1:n.*1464T>C
|
|
ENST00000643925.1:c.1612T>C
|
|
|
ENST00000644447.1:c.1844T>C
|
ENSP00000496282.1:p.Phe615Ser
|
|
ENST00000644484.1:c.*1743T>C
|
ENSP00000493558.1:n.*1743T>C
|
|
ENST00000644675.1:c.*1660T>C
|
ENSP00000494567.1:n.*1660T>C
|
|
ENST00000644757.1:c.*1773T>C
|
ENSP00000495085.1:n.*1773T>C
|
|
ENST00000644772.1:c.3554T>C
|
ENSP00000494321.1:p.Phe1185Ser
|
|
ENST00000645004.1:n.627T>C
|
|
|
ENST00000645076.1:c.2687T>C
|
|
|
ENST00000645417.1:c.654T>C
|
|
|
ENST00000645744.1:c.*1752T>C
|
ENSP00000494564.1:n.*1752T>C
|
|
ENST00000645760.1:c.3763T>C
|
|
|
ENST00000645884.1:c.*625T>C
|
ENSP00000495516.1:n.*625T>C
|
|
ENST00000646003.1:c.*1444T>C
|
ENSP00000495259.1:n.*1444T>C
|
|
ENST00000646207.1:c.*1955T>C
|
ENSP00000495025.1:n.*1955T>C
|
|
ENST00000646276.1:c.*1761T>C
|
ENSP00000496070.1:n.*1761T>C
|
|
ENST00000646592.1:c.2794T>C
|
|
|
ENST00000646902.1:c.3485T>C
|
ENSP00000494101.1:p.Phe1162Ser
|
|
ENST00000646993.1:c.*1884T>C
|
ENSP00000493720.1:n.*1884T>C
|
|
ENST00000647013.1:c.3494T>C
|
ENSP00000496741.1:n.3494T>C
|
|
ENST00000647015.1:c.3239T>C
|
ENSP00000495389.1:p.Phe1080Ser
|
|
ENST00000647086.1:c.*3218T>C
|
ENSP00000493677.1:n.*3218T>C
|
|
ENST00000647158.1:c.*1629T>C
|
ENSP00000495744.1:n.*1629T>C
|
|
ENST00000302539.8:c.3491T>C
|
ENSP00000303960.4:p.Phe1164Ser
|
|
ENST00000389817.7:c.3488T>C
|
ENSP00000374467.3:p.Phe1163Ser
|
|
ENST00000524561.1:n.620T>C
|
|
|
ENST00000527905.5:c.*364T>C
|
ENSP00000431653.1:n.*364T>C
|
|
NM_000352.4:c.3488T>C
|
NP_000343.2:p.Phe1163Ser
|
|
NM_001287174.1:c.3491T>C
|
NP_001274103.1:p.Phe1164Ser
|
|
XM_011520331.1:c.3488T>C
|
XP_011518633.1:p.Phe1163Ser
|
|
XM_011520332.1:c.3491T>C
|
XP_011518634.1:p.Phe1164Ser
|
|
XM_011520333.1:c.1988T>C
|
XP_011518635.1:p.Phe663Ser
|
|
XR_930890.1:n.3554T>C
|
|
|
XR_930892.1:n.3454T>C
|
|
|
XR_930893.1:n.3451T>C
|
|
|
NM_001351295.1:c.3554T>C
|
NP_001338224.1:p.Phe1185Ser
|
|
NM_001351296.1:c.3488T>C
|
NP_001338225.1:p.Phe1163Ser
|
|
NM_001351297.1:c.3485T>C
|
NP_001338226.1:p.Phe1162Ser
|
|
NR_147094.1:n.3637T>C
|
|
|
XM_017018197.2:c.3557T>C
|
XP_016873686.1:p.Phe1186Ser
|
|
XM_017018199.1:c.3554T>C
|
XP_016873688.1:p.Phe1185Ser
|
|
XM_017018201.2:c.3557T>C
|
XP_016873690.1:p.Phe1186Ser
|
|
XM_017018202.1:c.2054T>C
|
XP_016873691.1:p.Phe685Ser
|
|
XM_017018204.1:c.1445T>C
|
XP_016873693.1:p.Phe482Ser
|
|
XM_024448668.1:c.1856T>C
|
XP_024304436.1:p.Phe619Ser
|
|
XR_001747945.2:n.3629T>C
|
|
|
XR_001747946.2:n.3560T>C
|
|
|
XR_002957189.1:n.3709T>C
|
|
|
NM_000352.6:c.3488T>C
MANE Select
|
NP_000343.2:p.Phe1163Ser
|
|
NM_001287174.2:c.3491T>C
|
NP_001274103.1:p.Phe1164Ser
|
|
NM_001351295.2:c.3554T>C
|
NP_001338224.1:p.Phe1185Ser
|
|
NM_001351296.2:c.3488T>C
|
NP_001338225.1:p.Phe1163Ser
|
|
NM_001351297.2:c.3485T>C
|
NP_001338226.1:p.Phe1162Ser
|
|
NR_147094.2:n.3637T>C
|
|
|
NM_001287174.3:c.3491T>C
|
NP_001274103.1:p.Phe1164Ser
|
|