ENST00000415928.6:c.665+1077A>T
|
ENSP00000388838.2:n.665+1077A>T
|
|
ENST00000435065.7:c.788A>T
|
ENSP00000402760.2:p.Tyr263Phe
|
|
ENST00000448810.6:c.716A>T
|
ENSP00000401860.2:p.Tyr239Phe
|
|
ENST00000686757.1:c.735A>T
|
ENSP00000510721.1:p.Leu245Phe
|
|
ENST00000687740.1:n.1876A>T
|
|
|
ENST00000688151.1:n.1908A>T
|
|
|
ENST00000689271.1:c.671+1071A>T
|
ENSP00000510797.1:n.671+1071A>T
|
|
ENST00000690900.1:c.687A>T
|
ENSP00000510703.1:p.Leu229Phe
|
|
ENST00000692212.1:n.542A>T
|
|
|
ENST00000692355.1:c.204+1090A>T
|
|
|
ENST00000692413.1:c.735A>T
|
ENSP00000509374.1:p.Leu245Phe
|
|
ENST00000692825.1:c.784A>T
|
ENSP00000509447.1:n.784A>T
|
|
ENST00000693308.1:c.729A>T
|
ENSP00000509770.1:p.Leu243Phe
|
|
ENST00000693763.1:n.1876A>T
|
|
|
ENST00000245407.8:c.716A>T
MANE Select
|
ENSP00000245407.3:p.Tyr239Phe
|
|
ENST00000245407.7:c.716A>T
|
ENSP00000245407.3:p.Tyr239Phe
|
|
ENST00000415928.5:c.485A>T
|
ENSP00000388838.1:p.Tyr162Phe
|
|
ENST00000435065.6:c.788A>T
|
ENSP00000402760.2:p.Tyr263Phe
|
|
ENST00000437841.6:c.*31A>T
|
ENSP00000400553.1:n.*31A>T
|
|
ENST00000448810.5:c.64A>T
|
|
|
ENST00000461013.5:n.8138A>T
|
|
|
NM_001308122.1:c.788A>T
|
NP_001295051.1:p.Tyr263Phe
|
|
NM_003060.3:c.716A>T
|
NP_003051.1:p.Tyr239Phe
|
|
XM_011543590.1:c.98A>T
|
XP_011541892.1:p.Tyr33Phe
|
|
XR_427718.1:n.1076A>T
|
|
|
XR_948290.1:n.1057A>T
|
|
|
XR_948291.1:n.1070A>T
|
|
|
XM_011543590.2:c.98A>T
|
XP_011541892.1:p.Tyr33Phe
|
|
XM_017009778.2:c.188A>T
|
XP_016865267.1:p.Tyr63Phe
|
|
XR_001742215.1:n.1057A>T
|
|
|
XR_001742216.1:n.1076A>T
|
|
|
XR_427718.2:n.1076A>T
|
|
|
XR_948290.2:n.1057A>T
|
|
|
XR_948291.2:n.1070A>T
|
|
|
NM_003060.4:c.716A>T
MANE Select
|
NP_003051.1:p.Tyr239Phe
|
|
NM_001308122.2:c.788A>T
|
NP_001295051.1:p.Tyr263Phe
|
|