ENST00000525341.2:c.761G=
|
|
|
ENST00000528641.7:c.595G=
|
ENSP00000434982.3:p.Asp199=
|
|
ENST00000529797.2:n.1296G=
|
|
|
ENST00000682324.1:c.469-543G=
|
ENSP00000508017.1:n.469-543G=
|
|
ENST00000682659.1:c.415G=
|
ENSP00000507351.1:p.Asp139=
|
|
ENST00000682699.1:c.784G=
|
ENSP00000507935.1:p.Asp262=
|
|
ENST00000683237.1:c.779+5G=
|
ENSP00000507343.1:n.779+5G=
|
|
ENST00000683856.1:c.607G=
|
ENSP00000507979.1:p.Asp203=
|
|
ENST00000684006.1:c.784G=
|
ENSP00000507269.1:p.Asp262=
|
|
ENST00000684657.1:c.604G=
|
ENSP00000507961.1:p.Asp202=
|
|
ENST00000279146.8:c.784G=
MANE Select
|
ENSP00000279146.3:p.Asp262=
|
|
ENST00000279146.7:c.784G=
|
ENSP00000279146.3:p.Asp262=
|
|
ENST00000525341.1:c.436G=
|
ENSP00000476993.1:p.Asp146=
|
|
ENST00000528641.6:c.595G=
|
ENSP00000434982.2:p.Asp199=
|
|
NM_001302959.1:c.607G=
|
NP_001289888.1:p.Asp203=
|
|
NM_001302960.1:c.779+5G=
|
NP_001289889.1:n.779+5G=
|
|
NM_003977.3:c.784G=
|
NP_003968.3:p.Asp262=
|
|
XM_024448761.1:c.784G=
|
XP_024304529.1:p.Asp262=
|
|
NM_003977.4:c.784G=
MANE Select
|
NP_003968.3:p.Asp262=
|
|
NM_001302960.2:c.779+5G=
|
NP_001289889.1:n.779+5G=
|
|
NM_001302959.2:c.607G=
|
NP_001289888.1:p.Asp203=
|
|