ENST00000525341.2:c.1163G=
|
|
|
ENST00000528641.7:c.667G=
|
ENSP00000434982.3:p.Ala223=
|
|
ENST00000529797.2:n.1698G=
|
|
|
ENST00000682324.1:c.469-141G=
|
ENSP00000508017.1:n.469-141G=
|
|
ENST00000682659.1:c.487G=
|
ENSP00000507351.1:p.Ala163=
|
|
ENST00000682699.1:c.856G=
|
ENSP00000507935.1:p.Ala286=
|
|
ENST00000683237.1:c.848G=
|
ENSP00000507343.1:p.Gly283=
|
|
ENST00000683856.1:c.679G=
|
ENSP00000507979.1:p.Ala227=
|
|
ENST00000684006.1:c.845G=
|
ENSP00000507269.1:p.Gly282=
|
|
ENST00000684657.1:c.676G=
|
ENSP00000507961.1:p.Ala226=
|
|
ENST00000279146.8:c.856G=
MANE Select
|
ENSP00000279146.3:p.Ala286=
|
|
ENST00000279146.7:c.856G=
|
ENSP00000279146.3:p.Ala286=
|
|
ENST00000528641.6:c.667G=
|
ENSP00000434982.2:p.Ala223=
|
|
NM_001302959.1:c.679G=
|
NP_001289888.1:p.Ala227=
|
|
NM_001302960.1:c.848G=
|
NP_001289889.1:p.Gly283=
|
|
NM_003977.3:c.856G=
|
NP_003968.3:p.Ala286=
|
|
XM_024448761.1:c.856G=
|
XP_024304529.1:p.Ala286=
|
|
NM_003977.4:c.856G=
MANE Select
|
NP_003968.3:p.Ala286=
|
|
NM_001302960.2:c.848G=
|
NP_001289889.1:p.Gly283=
|
|
NM_001302959.2:c.679G=
|
NP_001289888.1:p.Ala227=
|
|