ENST00000415928.6:c.1088T>C
|
ENSP00000388838.2:p.Phe363Ser
|
|
ENST00000435065.7:c.1319T>C
|
ENSP00000402760.2:p.Phe440Ser
|
|
ENST00000448810.6:c.*99T>C
|
ENSP00000401860.2:n.*99T>C
|
|
ENST00000685543.1:n.1388T>C
|
|
|
ENST00000686757.1:c.*411T>C
|
ENSP00000510721.1:n.*411T>C
|
|
ENST00000687740.1:n.3932T>C
|
|
|
ENST00000688151.1:n.2557T>C
|
|
|
ENST00000689271.1:c.1094T>C
|
ENSP00000510797.1:p.Phe365Ser
|
|
ENST00000690900.1:c.*411T>C
|
ENSP00000510703.1:n.*411T>C
|
|
ENST00000692212.1:n.2859T>C
|
|
|
ENST00000692355.1:c.500T>C
|
|
|
ENST00000692413.1:c.1229T>C
|
ENSP00000509374.1:p.Phe410Ser
|
|
ENST00000692825.1:c.1315T>C
|
ENSP00000509447.1:n.1315T>C
|
|
ENST00000693308.1:c.1295T>C
|
ENSP00000509770.1:p.Phe432Ser
|
|
ENST00000693763.1:n.2407T>C
|
|
|
ENST00000245407.8:c.1247T>C
MANE Select
|
ENSP00000245407.3:p.Phe416Ser
|
|
ENST00000245407.7:c.1247T>C
|
ENSP00000245407.3:p.Phe416Ser
|
|
ENST00000435065.6:c.1319T>C
|
ENSP00000402760.2:p.Phe440Ser
|
|
ENST00000447841.5:c.112-1549T>C
|
|
|
ENST00000448810.5:c.509T>C
|
|
|
ENST00000461013.5:n.8669T>C
|
|
|
ENST00000475308.1:n.1925T>C
|
|
|
ENST00000479605.5:n.350T>C
|
|
|
NM_001308122.1:c.1319T>C
|
NP_001295051.1:p.Phe440Ser
|
|
NM_003060.3:c.1247T>C
|
NP_003051.1:p.Phe416Ser
|
|
XM_011543590.1:c.629T>C
|
XP_011541892.1:p.Phe210Ser
|
|
XR_427718.1:n.1607T>C
|
|
|
XR_948290.1:n.1394-1549T>C
|
|
|
XR_948291.1:n.1601T>C
|
|
|
XM_011543590.2:c.629T>C
|
XP_011541892.1:p.Phe210Ser
|
|
XM_017009778.2:c.719T>C
|
XP_016865267.1:p.Phe240Ser
|
|
XR_001742215.1:n.1502T>C
|
|
|
XR_001742216.1:n.1521T>C
|
|
|
XR_427718.2:n.1607T>C
|
|
|
XR_948290.2:n.1394-1549T>C
|
|
|
XR_948291.2:n.1601T>C
|
|
|
NM_003060.4:c.1247T>C
MANE Select
|
NP_003051.1:p.Phe416Ser
|
|
NM_001308122.2:c.1319T>C
|
NP_001295051.1:p.Phe440Ser
|
|