|
ENST00000370683.6:c.673T>C
MANE Select
|
ENSP00000359717.1:p.Cys225Arg
|
|
|
ENST00000394155.8:c.625T>C
MANE Plus Clinical
|
ENSP00000377710.2:p.Cys209Arg
|
|
|
ENST00000628919.3:c.625T>C
|
ENSP00000487147.2:p.Cys209Arg
|
|
|
ENST00000651089.1:c.625T>C
|
ENSP00000498684.1:p.Cys209Arg
|
|
|
ENST00000651929.2:c.625T>C
|
ENSP00000499016.1:p.Cys209Arg
|
|
|
ENST00000652457.1:c.625T>C
|
ENSP00000498503.1:p.Cys209Arg
|
|
|
ENST00000345434.7:c.625T>C
|
ENSP00000071281.6:p.Cys209Arg
|
|
|
ENST00000370674.3:c.625T>C
|
ENSP00000359708.1:p.Cys209Arg
|
|
|
ENST00000370676.7:c.549+617T>C
|
ENSP00000359710.3:n.549+617T>C
|
|
|
ENST00000370683.5:c.673T>C
|
ENSP00000359717.1:p.Cys225Arg
|
|
|
ENST00000370690.7:c.625T>C
|
ENSP00000359724.3:p.Cys209Arg
|
|
|
ENST00000394153.6:c.625T>C
|
ENSP00000377709.2:p.Cys209Arg
|
|
|
ENST00000394155.6:c.625T>C
|
ENSP00000377710.2:p.Cys209Arg
|
|
|
ENST00000535737.5:c.625T>C
|
ENSP00000444815.1:p.Cys209Arg
|
|
|
ENST00000539015.5:c.712T>C
|
ENSP00000437673.1:p.Cys238Arg
|
|
|
ENST00000543669.5:c.625T>C
|
ENSP00000443333.1:p.Cys209Arg
|
|
|
ENST00000618438.4:c.501+617T>C
|
ENSP00000477609.1:n.501+617T>C
|
|
|
ENST00000626004.1:n.329T>C
|
|
|
|
ENST00000628568.1:c.625T>C
|
ENSP00000486782.1:p.Cys209Arg
|
|
|
ENST00000629039.2:c.625T>C
|
ENSP00000486439.1:p.Cys209Arg
|
|
|
ENST00000630084.2:c.625T>C
|
ENSP00000485897.1:p.Cys209Arg
|
|
|
NM_001159699.1:c.673T>C
|
NP_001153171.1:p.Cys225Arg
|
|
|
NM_001159700.1:c.625T>C
|
NP_001153172.1:p.Cys209Arg
|
|
|
NM_001159701.1:c.712T>C
|
NP_001153173.1:p.Cys238Arg
|
|
|
NM_001159702.2:c.625T>C
|
NP_001153174.1:p.Cys209Arg
|
|
|
NM_001159703.1:c.501+617T>C
|
NP_001153175.1:n.501+617T>C
|
|
|
NM_001159704.1:c.625T>C
|
NP_001153176.1:p.Cys209Arg
|
|
|
NM_001167819.1:c.625T>C
|
NP_001161291.1:p.Cys209Arg
|
|
|
NM_001449.4:c.625T>C
|
NP_001440.2:p.Cys209Arg
|
|
|
NR_027621.1:n.1036T>C
|
|
|
|
XM_006724743.2:c.673T>C
|
XP_006724806.1:p.Cys225Arg
|
|
|
XM_006724744.2:c.625T>C
|
XP_006724807.1:p.Cys209Arg
|
|
|
XM_006724745.2:c.625T>C
|
XP_006724808.1:p.Cys209Arg
|
|
|
XM_006724746.2:c.625T>C
|
XP_006724809.1:p.Cys209Arg
|
|
|
XM_006724747.2:c.625T>C
|
XP_006724810.1:p.Cys209Arg
|
|
|
XM_011531316.1:c.549+617T>C
|
XP_011529618.1:n.549+617T>C
|
|
|
NM_001330659.1:c.549+617T>C
|
NP_001317588.1:n.549+617T>C
|
|
|
XM_006724744.3:c.625T>C
|
XP_006724807.1:p.Cys209Arg
|
|
|
XM_006724745.4:c.625T>C
|
XP_006724808.1:p.Cys209Arg
|
|
|
XM_006724746.3:c.625T>C
|
XP_006724809.1:p.Cys209Arg
|
|
|
XM_006724747.3:c.625T>C
|
XP_006724810.1:p.Cys209Arg
|
|
|
XM_017029357.2:c.625T>C
|
XP_016884846.1:p.Cys209Arg
|
|
|
XM_024452353.1:c.625T>C
|
XP_024308121.1:p.Cys209Arg
|
|
|
XM_024452354.1:c.625T>C
|
XP_024308122.1:p.Cys209Arg
|
|
|
XM_024452355.1:c.625T>C
|
XP_024308123.1:p.Cys209Arg
|
|
|
NM_001449.5:c.625T>C
|
NP_001440.2:p.Cys209Arg
|
|
|
NM_001159699.2:c.673T>C
MANE Select
|
NP_001153171.1:p.Cys225Arg
|
|
|
NM_001159700.2:c.625T>C
|
NP_001153172.1:p.Cys209Arg
|
|
|
NM_001159701.2:c.712T>C
|
NP_001153173.1:p.Cys238Arg
|
|
|
NM_001159702.3:c.625T>C
MANE Plus Clinical
|
NP_001153174.1:p.Cys209Arg
|
|
|
NM_001159703.2:c.501+617T>C
|
NP_001153175.1:n.501+617T>C
|
|
|
NM_001330659.2:c.549+617T>C
|
NP_001317588.1:n.549+617T>C
|
|
|
NM_001369326.1:c.625T>C
|
NP_001356255.1:p.Cys209Arg
|
|
|
NM_001369327.1:c.625T>C
|
NP_001356256.1:p.Cys209Arg
|
|
|
NM_001369328.1:c.625T>C
|
NP_001356257.1:p.Cys209Arg
|
|
|
NM_001369329.1:c.625T>C
|
NP_001356258.1:p.Cys209Arg
|
|
|
NM_001369330.1:c.625T>C
|
NP_001356259.1:p.Cys209Arg
|
|
|
NM_001369331.1:c.625T>C
|
NP_001356260.1:p.Cys209Arg
|
|
|
NM_001369327.2:c.625T>C
|
NP_001356256.1:p.Cys209Arg
|
|
|
NR_027621.2:n.1036T>C
|
|
|
