ENST00000525341.2:c.1165T>G
|
|
|
ENST00000528641.7:c.669T>G
|
ENSP00000434982.3:p.Ala223=
|
|
ENST00000529797.2:n.1700T>G
|
|
|
ENST00000682324.1:c.469-139T>G
|
ENSP00000508017.1:n.469-139T>G
|
|
ENST00000682659.1:c.489T>G
|
ENSP00000507351.1:p.Ala163=
|
|
ENST00000682699.1:c.858T>G
|
ENSP00000507935.1:p.Ala286=
|
|
ENST00000683237.1:c.850T>G
|
ENSP00000507343.1:p.Ter284Gly
|
|
ENST00000683856.1:c.681T>G
|
ENSP00000507979.1:p.Ala227=
|
|
ENST00000684006.1:c.847T>G
|
ENSP00000507269.1:p.Ter283Gly
|
|
ENST00000684657.1:c.678T>G
|
ENSP00000507961.1:p.Ala226=
|
|
ENST00000279146.8:c.858T>G
MANE Select
|
ENSP00000279146.3:p.Ala286=
|
|
ENST00000279146.7:c.858T>G
|
ENSP00000279146.3:p.Ala286=
|
|
ENST00000528641.6:c.669T>G
|
ENSP00000434982.2:p.Ala223=
|
|
NM_001302959.1:c.681T>G
|
NP_001289888.1:p.Ala227=
|
|
NM_001302960.1:c.850T>G
|
NP_001289889.1:p.Ter284Gly
|
|
NM_003977.3:c.858T>G
|
NP_003968.3:p.Ala286=
|
|
XM_024448761.1:c.858T>G
|
XP_024304529.1:p.Ala286=
|
|
NM_003977.4:c.858T>G
MANE Select
|
NP_003968.3:p.Ala286=
|
|
NM_001302960.2:c.850T>G
|
NP_001289889.1:p.Ter284Gly
|
|
NM_001302959.2:c.681T>G
|
NP_001289888.1:p.Ala227=
|
|