ENST00000415928.6:c.665+1017C>G
|
ENSP00000388838.2:n.665+1017C>G
|
|
ENST00000435065.7:c.728C>G
|
ENSP00000402760.2:p.Thr243Arg
|
|
ENST00000448810.6:c.656C>G
|
ENSP00000401860.2:p.Thr219Arg
|
|
ENST00000686757.1:c.675C>G
|
ENSP00000510721.1:p.Asp225Glu
|
|
ENST00000687740.1:n.1816C>G
|
|
|
ENST00000688151.1:n.1848C>G
|
|
|
ENST00000689271.1:c.671+1011C>G
|
ENSP00000510797.1:n.671+1011C>G
|
|
ENST00000690900.1:c.672-45C>G
|
ENSP00000510703.1:n.672-45C>G
|
|
ENST00000692212.1:n.482C>G
|
|
|
ENST00000692355.1:c.204+1030C>G
|
|
|
ENST00000692413.1:c.675C>G
|
ENSP00000509374.1:p.Asp225Glu
|
|
ENST00000692825.1:c.724C>G
|
ENSP00000509447.1:n.724C>G
|
|
ENST00000693308.1:c.669C>G
|
ENSP00000509770.1:p.Asp223Glu
|
|
ENST00000693763.1:n.1816C>G
|
|
|
ENST00000245407.8:c.656C>G
MANE Select
|
ENSP00000245407.3:p.Thr219Arg
|
|
ENST00000245407.7:c.656C>G
|
ENSP00000245407.3:p.Thr219Arg
|
|
ENST00000415928.5:c.425C>G
|
ENSP00000388838.1:p.Thr142Arg
|
|
ENST00000435065.6:c.728C>G
|
ENSP00000402760.2:p.Thr243Arg
|
|
ENST00000437841.6:c.397C>G
|
ENSP00000400553.1:p.Gln133Glu
|
|
ENST00000448810.5:c.4C>G
|
|
|
ENST00000461013.5:n.8078C>G
|
|
|
NM_001308122.1:c.728C>G
|
NP_001295051.1:p.Thr243Arg
|
|
NM_003060.3:c.656C>G
|
NP_003051.1:p.Thr219Arg
|
|
XM_011543590.1:c.38C>G
|
XP_011541892.1:p.Thr13Arg
|
|
XR_427718.1:n.1016C>G
|
|
|
XR_948290.1:n.997C>G
|
|
|
XR_948291.1:n.1010C>G
|
|
|
XM_011543590.2:c.38C>G
|
XP_011541892.1:p.Thr13Arg
|
|
XM_017009778.2:c.128C>G
|
XP_016865267.1:p.Thr43Arg
|
|
XR_001742215.1:n.997C>G
|
|
|
XR_001742216.1:n.1016C>G
|
|
|
XR_427718.2:n.1016C>G
|
|
|
XR_948290.2:n.997C>G
|
|
|
XR_948291.2:n.1010C>G
|
|
|
NM_003060.4:c.656C>G
MANE Select
|
NP_003051.1:p.Thr219Arg
|
|
NM_001308122.2:c.728C>G
|
NP_001295051.1:p.Thr243Arg
|
|