|
ENST00000461271.6:c.303G=
|
ENSP00000464056.2:p.Glu101=
|
|
|
ENST00000697677.1:n.1735G=
|
|
|
|
ENST00000697678.1:n.556G=
|
|
|
|
ENST00000697679.1:n.1728G=
|
|
|
|
ENST00000697680.1:c.*1518G=
|
ENSP00000513392.1:n.*1518G=
|
|
|
ENST00000697681.1:c.*1670G=
|
ENSP00000513393.1:n.*1670G=
|
|
|
ENST00000697683.1:c.*1518G=
|
ENSP00000513395.1:n.*1518G=
|
|
|
ENST00000697684.1:n.714G=
|
|
|
|
ENST00000697685.1:c.*1351G=
|
ENSP00000513396.1:n.*1351G=
|
|
|
ENST00000697686.1:c.303G=
|
ENSP00000513397.1:p.Glu101=
|
|
|
ENST00000697687.1:n.533G=
|
|
|
|
ENST00000697688.1:n.700G=
|
|
|
|
ENST00000697689.1:c.*1190G=
|
ENSP00000513398.1:n.*1190G=
|
|
|
ENST00000697690.1:c.654G=
|
ENSP00000513399.1:p.Glu218=
|
|
|
ENST00000697691.1:c.*626G=
|
ENSP00000513400.1:n.*626G=
|
|
|
ENST00000697692.1:c.*666G=
|
ENSP00000513401.1:n.*666G=
|
|
|
ENST00000697694.1:c.303G=
|
ENSP00000513402.1:p.Glu101=
|
|
|
ENST00000697695.1:n.1261G=
|
|
|
|
ENST00000337432.9:c.654G=
MANE Select
|
ENSP00000336701.4:p.Glu218=
|
|
|
ENST00000337432.8:c.654G=
|
ENSP00000336701.4:p.Glu218=
|
|
|
ENST00000413590.5:c.292G=
|
|
|
|
ENST00000425173.5:c.450G=
|
ENSP00000407282.1:p.Glu150=
|
|
|
ENST00000461271.5:c.303G=
|
ENSP00000464056.1:p.Glu101=
|
|
|
ENST00000475762.5:c.*1357G=
|
ENSP00000432421.1:n.*1357G=
|
|
|
ENST00000482007.5:c.*82G=
|
ENSP00000433332.1:n.*82G=
|
|
|
ENST00000487525.5:c.*82G=
|
ENSP00000431637.1:n.*82G=
|
|
|
ENST00000487921.5:n.566G=
|
|
|
|
ENST00000583539.5:c.654G=
|
ENSP00000463121.1:p.Glu218=
|
|
|
ENST00000584617.5:c.376G=
|
|
|
|
NM_058216.2:c.654G=
|
NP_478123.1:p.Glu218=
|
|
|
NR_103872.1:n.558G=
|
|
|
|
XM_006722001.2:c.654G=
|
XP_006722064.1:p.Glu218=
|
|
|
XM_006722002.2:c.654G=
|
XP_006722065.1:p.Glu218=
|
|
|
XM_006722004.2:c.303G=
|
XP_006722067.1:p.Glu101=
|
|
|
XM_006722005.2:c.303G=
|
XP_006722068.1:p.Glu101=
|
|
|
XM_011525092.1:c.303G=
|
XP_011523394.1:p.Glu101=
|
|
|
XM_011525093.1:c.303G=
|
XP_011523395.1:p.Glu101=
|
|
|
XM_011525094.1:c.303G=
|
XP_011523396.1:p.Glu101=
|
|
|
XR_934513.1:n.727G=
|
|
|
|
XR_934514.1:n.727G=
|
|
|
|
XM_006722001.4:c.654G=
|
XP_006722064.1:p.Glu218=
|
|
|
XM_006722002.4:c.654G=
|
XP_006722065.1:p.Glu218=
|
|
|
XM_006722004.3:c.303G=
|
XP_006722067.1:p.Glu101=
|
|
|
XM_006722005.3:c.303G=
|
XP_006722068.1:p.Glu101=
|
|
|
XM_011525092.2:c.303G=
|
XP_011523394.1:p.Glu101=
|
|
|
XM_011525093.2:c.303G=
|
XP_011523395.1:p.Glu101=
|
|
|
XM_011525094.2:c.303G=
|
XP_011523396.1:p.Glu101=
|
|
|
XM_017024914.1:c.303G=
|
XP_016880403.1:p.Glu101=
|
|
|
XM_017024915.1:c.303G=
|
XP_016880404.1:p.Glu101=
|
|
|
XM_017024916.1:c.303G=
|
XP_016880405.1:p.Glu101=
|
|
|
XM_017024917.1:c.303G=
|
XP_016880406.1:p.Glu101=
|
|
|
XM_017024918.2:c.303G=
|
XP_016880407.1:p.Glu101=
|
|
|
XM_017024919.1:c.303G=
|
XP_016880408.1:p.Glu101=
|
|
|
XR_934513.3:n.1158G=
|
|
|
|
XR_934514.3:n.1158G=
|
|
|
|
NM_058216.3:c.654G=
MANE Select
|
NP_478123.1:p.Glu218=
|
|
|
NR_103872.2:n.529G=
|
|
|
