ENST00000415928.6:c.665+1042T>C
|
ENSP00000388838.2:n.665+1042T>C
|
|
ENST00000435065.7:c.753T>C
|
ENSP00000402760.2:p.Arg251=
|
|
ENST00000448810.6:c.681T>C
|
ENSP00000401860.2:p.Arg227=
|
|
ENST00000686757.1:c.700T>C
|
ENSP00000510721.1:p.Tyr234His
|
|
ENST00000687740.1:n.1841T>C
|
|
|
ENST00000688151.1:n.1873T>C
|
|
|
ENST00000689271.1:c.671+1036T>C
|
ENSP00000510797.1:n.671+1036T>C
|
|
ENST00000690900.1:c.672-20T>C
|
ENSP00000510703.1:n.672-20T>C
|
|
ENST00000692212.1:n.507T>C
|
|
|
ENST00000692355.1:c.204+1055T>C
|
|
|
ENST00000692413.1:c.700T>C
|
ENSP00000509374.1:p.Tyr234His
|
|
ENST00000692825.1:c.749T>C
|
ENSP00000509447.1:n.749T>C
|
|
ENST00000693308.1:c.694T>C
|
ENSP00000509770.1:p.Tyr232His
|
|
ENST00000693763.1:n.1841T>C
|
|
|
ENST00000245407.8:c.681T>C
MANE Select
|
ENSP00000245407.3:p.Arg227=
|
|
ENST00000245407.7:c.681T>C
|
ENSP00000245407.3:p.Arg227=
|
|
ENST00000415928.5:c.450T>C
|
ENSP00000388838.1:p.Arg150=
|
|
ENST00000435065.6:c.753T>C
|
ENSP00000402760.2:p.Arg251=
|
|
ENST00000437841.6:c.422T>C
|
ENSP00000400553.1:p.Val141Ala
|
|
ENST00000448810.5:c.29T>C
|
|
|
ENST00000461013.5:n.8103T>C
|
|
|
NM_001308122.1:c.753T>C
|
NP_001295051.1:p.Arg251=
|
|
NM_003060.3:c.681T>C
|
NP_003051.1:p.Arg227=
|
|
XM_011543590.1:c.63T>C
|
XP_011541892.1:p.Arg21=
|
|
XR_427718.1:n.1041T>C
|
|
|
XR_948290.1:n.1022T>C
|
|
|
XR_948291.1:n.1035T>C
|
|
|
XM_011543590.2:c.63T>C
|
XP_011541892.1:p.Arg21=
|
|
XM_017009778.2:c.153T>C
|
XP_016865267.1:p.Arg51=
|
|
XR_001742215.1:n.1022T>C
|
|
|
XR_001742216.1:n.1041T>C
|
|
|
XR_427718.2:n.1041T>C
|
|
|
XR_948290.2:n.1022T>C
|
|
|
XR_948291.2:n.1035T>C
|
|
|
NM_003060.4:c.681T>C
MANE Select
|
NP_003051.1:p.Arg227=
|
|
NM_001308122.2:c.753T>C
|
NP_001295051.1:p.Arg251=
|
|