ENST00000525341.2:c.1273C>G
|
|
|
ENST00000528641.7:c.777C>G
|
ENSP00000434982.3:p.Ala259=
|
|
ENST00000529797.2:n.1808C>G
|
|
|
ENST00000682324.1:c.469-31C>G
|
ENSP00000508017.1:n.469-31C>G
|
|
ENST00000682659.1:c.597C>G
|
ENSP00000507351.1:p.Ala199=
|
|
ENST00000683237.1:c.*106C>G
|
ENSP00000507343.1:n.*106C>G
|
|
ENST00000683856.1:c.789C>G
|
ENSP00000507979.1:p.Ala263=
|
|
ENST00000684006.1:c.*106C>G
|
ENSP00000507269.1:n.*106C>G
|
|
ENST00000684657.1:c.786C>G
|
ENSP00000507961.1:p.Ala262=
|
|
ENST00000279146.8:c.966C>G
MANE Select
|
ENSP00000279146.3:p.Ala322=
|
|
ENST00000279146.7:c.966C>G
|
ENSP00000279146.3:p.Ala322=
|
|
NM_001302959.1:c.789C>G
|
NP_001289888.1:p.Ala263=
|
|
NM_001302960.1:c.*106C>G
|
NP_001289889.1:n.*106C>G
|
|
NM_003977.3:c.966C>G
|
NP_003968.3:p.Ala322=
|
|
XM_024448761.1:c.966C>G
|
XP_024304529.1:p.Ala322=
|
|
NM_003977.4:c.966C>G
MANE Select
|
NP_003968.3:p.Ala322=
|
|
NM_001302960.2:c.*106C>G
|
NP_001289889.1:n.*106C>G
|
|
NM_001302959.2:c.789C>G
|
NP_001289888.1:p.Ala263=
|
|