ENST00000525341.2:c.882G>C
|
|
|
ENST00000528641.7:c.598+118G>C
|
ENSP00000434982.3:n.598+118G>C
|
|
ENST00000529797.2:n.1417G>C
|
|
|
ENST00000682324.1:c.469-422G>C
|
ENSP00000508017.1:n.469-422G>C
|
|
ENST00000682659.1:c.418+118G>C
|
ENSP00000507351.1:n.418+118G>C
|
|
ENST00000682699.1:c.787+118G>C
|
ENSP00000507935.1:n.787+118G>C
|
|
ENST00000683237.1:c.779+126G>C
|
ENSP00000507343.1:n.779+126G>C
|
|
ENST00000683856.1:c.610+118G>C
|
ENSP00000507979.1:n.610+118G>C
|
|
ENST00000684006.1:c.787+118G>C
|
ENSP00000507269.1:n.787+118G>C
|
|
ENST00000684657.1:c.607+118G>C
|
ENSP00000507961.1:n.607+118G>C
|
|
ENST00000279146.8:c.787+118G>C
MANE Select
|
ENSP00000279146.3:n.787+118G>C
|
|
ENST00000279146.7:c.787+118G>C
|
ENSP00000279146.3:n.787+118G>C
|
|
ENST00000525341.1:c.557G>C
|
ENSP00000476993.1:p.Gly186Ala
|
|
ENST00000528641.6:c.598+118G>C
|
ENSP00000434982.2:n.598+118G>C
|
|
NM_001302959.1:c.610+118G>C
|
NP_001289888.1:n.610+118G>C
|
|
NM_001302960.1:c.779+126G>C
|
NP_001289889.1:n.779+126G>C
|
|
NM_003977.3:c.787+118G>C
|
NP_003968.3:n.787+118G>C
|
|
XM_024448761.1:c.787+118G>C
|
XP_024304529.1:n.787+118G>C
|
|
NM_003977.4:c.787+118G>C
MANE Select
|
NP_003968.3:n.787+118G>C
|
|
NM_001302960.2:c.779+126G>C
|
NP_001289889.1:n.779+126G>C
|
|
NM_001302959.2:c.610+118G>C
|
NP_001289888.1:n.610+118G>C
|
|