ENST00000525341.2:c.361T>G
|
|
|
ENST00000528641.7:c.280-667T>G
|
ENSP00000434982.3:n.280-667T>G
|
|
ENST00000529797.2:n.314T>G
|
|
|
ENST00000682324.1:c.384T>G
|
ENSP00000508017.1:p.Arg128=
|
|
ENST00000682659.1:c.100-667T>G
|
ENSP00000507351.1:n.100-667T>G
|
|
ENST00000682699.1:c.384T>G
|
ENSP00000507935.1:p.Arg128=
|
|
ENST00000683237.1:c.384T>G
|
ENSP00000507343.1:p.Arg128=
|
|
ENST00000683856.1:c.207T>G
|
ENSP00000507979.1:p.Arg69=
|
|
ENST00000684006.1:c.384T>G
|
ENSP00000507269.1:p.Arg128=
|
|
ENST00000684657.1:c.204T>G
|
ENSP00000507961.1:p.Arg68=
|
|
ENST00000279146.8:c.384T>G
MANE Select
|
ENSP00000279146.3:p.Arg128=
|
|
ENST00000279146.7:c.384T>G
|
ENSP00000279146.3:p.Arg128=
|
|
ENST00000525341.1:c.36T>G
|
ENSP00000476993.1:p.Arg12=
|
|
ENST00000528641.6:c.280-667T>G
|
ENSP00000434982.2:n.280-667T>G
|
|
ENST00000529797.1:n.494T>G
|
|
|
NM_001302959.1:c.207T>G
|
NP_001289888.1:p.Arg69=
|
|
NM_001302960.1:c.384T>G
|
NP_001289889.1:p.Arg128=
|
|
NM_003977.3:c.384T>G
|
NP_003968.3:p.Arg128=
|
|
XM_024448761.1:c.384T>G
|
XP_024304529.1:p.Arg128=
|
|
NM_003977.4:c.384T>G
MANE Select
|
NP_003968.3:p.Arg128=
|
|
NM_001302960.2:c.384T>G
|
NP_001289889.1:p.Arg128=
|
|
NM_001302959.2:c.207T>G
|
NP_001289888.1:p.Arg69=
|
|