|
NM_003060.4:c.1073A>G
MANE Select
|
NP_003051.1:p.Tyr358Cys
|
|
ENST00000245407.8:c.1073A>G
MANE Select
|
ENSP00000245407.3:p.Tyr358Cys
|
|
NM_001308122.1:c.1145A>G
|
NP_001295051.1:p.Tyr382Cys
|
|
NM_001308122.2:c.1145A>G
|
NP_001295051.1:p.Tyr382Cys
|
|
NM_003060.3:c.1073A>G
|
NP_003051.1:p.Tyr358Cys
|
|
ENST00000245407.7:c.1073A>G
|
ENSP00000245407.3:p.Tyr358Cys
|
|
ENST00000415928.6:c.914A>G
|
ENSP00000388838.2:p.Tyr305Cys
|
|
ENST00000435065.6:c.1145A>G
|
ENSP00000402760.2:p.Tyr382Cys
|
|
ENST00000435065.7:c.1145A>G
|
ENSP00000402760.2:p.Tyr382Cys
|
|
ENST00000447841.5:c.111+1689A>G
|
|
|
ENST00000448810.5:c.401-66A>G
|
|
|
ENST00000448810.6:c.1053-66A>G
|
ENSP00000401860.2:n.1053-66A>G
|
|
ENST00000461013.5:n.8495A>G
|
|
|
ENST00000475308.1:n.1751A>G
|
|
|
ENST00000479605.5:n.176A>G
|
|
|
ENST00000685543.1:n.1214A>G
|
|
|
ENST00000686757.1:c.*237A>G
|
ENSP00000510721.1:n.*237A>G
|
|
ENST00000687740.1:n.3758A>G
|
|
|
ENST00000688151.1:n.2383A>G
|
|
|
ENST00000689271.1:c.920A>G
|
ENSP00000510797.1:p.Tyr307Cys
|
|
ENST00000690900.1:c.*237A>G
|
ENSP00000510703.1:n.*237A>G
|
|
ENST00000692212.1:n.2685A>G
|
|
|
ENST00000692355.1:c.326A>G
|
|
|
ENST00000692413.1:c.1055A>G
|
ENSP00000509374.1:p.Tyr352Cys
|
|
ENST00000692825.1:c.1141A>G
|
ENSP00000509447.1:n.1141A>G
|
|
ENST00000693308.1:c.1121A>G
|
ENSP00000509770.1:p.Tyr374Cys
|
|
ENST00000693763.1:n.2233A>G
|
|
|
XM_011543590.1:c.455A>G
|
XP_011541892.1:p.Tyr152Cys
|
|
XM_011543590.2:c.455A>G
|
XP_011541892.1:p.Tyr152Cys
|
|
XM_017009778.2:c.545A>G
|
XP_016865267.1:p.Tyr182Cys
|
|
XR_001742215.1:n.1394-66A>G
|
|
|
XR_001742216.1:n.1413-66A>G
|
|
|
XR_427718.1:n.1433A>G
|
|
|
XR_427718.2:n.1433A>G
|
|
|
XR_948290.1:n.1393+1689A>G
|
|
|
XR_948290.2:n.1393+1689A>G
|
|
|
XR_948291.1:n.1427A>G
|
|
|
XR_948291.2:n.1427A>G
|
|
