ENST00000415928.6:c.798A>T
|
ENSP00000388838.2:p.Gln266His
|
|
ENST00000435065.7:c.1029A>T
|
ENSP00000402760.2:p.Gln343His
|
|
ENST00000448810.6:c.957A>T
|
ENSP00000401860.2:p.Gln319His
|
|
ENST00000685543.1:n.1098A>T
|
|
|
ENST00000686757.1:c.*121A>T
|
ENSP00000510721.1:n.*121A>T
|
|
ENST00000687740.1:n.3642A>T
|
|
|
ENST00000688151.1:n.2267A>T
|
|
|
ENST00000689271.1:c.804A>T
|
ENSP00000510797.1:p.Gln268His
|
|
ENST00000690900.1:c.*121A>T
|
ENSP00000510703.1:n.*121A>T
|
|
ENST00000692212.1:n.901A>T
|
|
|
ENST00000692355.1:c.210A>T
|
|
|
ENST00000692413.1:c.939A>T
|
ENSP00000509374.1:p.Gln313His
|
|
ENST00000692825.1:c.1025A>T
|
ENSP00000509447.1:n.1025A>T
|
|
ENST00000693308.1:c.1005A>T
|
ENSP00000509770.1:p.Gln335His
|
|
ENST00000693763.1:n.2117A>T
|
|
|
ENST00000245407.8:c.957A>T
MANE Select
|
ENSP00000245407.3:p.Gln319His
|
|
ENST00000245407.7:c.957A>T
|
ENSP00000245407.3:p.Gln319His
|
|
ENST00000435065.6:c.1029A>T
|
ENSP00000402760.2:p.Gln343His
|
|
ENST00000437841.6:c.*272A>T
|
ENSP00000400553.1:n.*272A>T
|
|
ENST00000447841.5:c.16A>T
|
|
|
ENST00000448810.5:c.305A>T
|
|
|
ENST00000461013.5:n.8379A>T
|
|
|
ENST00000479605.5:n.60A>T
|
|
|
NM_001308122.1:c.1029A>T
|
NP_001295051.1:p.Gln343His
|
|
NM_003060.3:c.957A>T
|
NP_003051.1:p.Gln319His
|
|
XM_011543590.1:c.339A>T
|
XP_011541892.1:p.Gln113His
|
|
XR_427718.1:n.1317A>T
|
|
|
XR_948290.1:n.1298A>T
|
|
|
XR_948291.1:n.1311A>T
|
|
|
XM_011543590.2:c.339A>T
|
XP_011541892.1:p.Gln113His
|
|
XM_017009778.2:c.429A>T
|
XP_016865267.1:p.Gln143His
|
|
XR_001742215.1:n.1298A>T
|
|
|
XR_001742216.1:n.1317A>T
|
|
|
XR_427718.2:n.1317A>T
|
|
|
XR_948290.2:n.1298A>T
|
|
|
XR_948291.2:n.1311A>T
|
|
|
NM_003060.4:c.957A>T
MANE Select
|
NP_003051.1:p.Gln319His
|
|
NM_001308122.2:c.1029A>T
|
NP_001295051.1:p.Gln343His
|
|