ENST00000681978.1:n.2678G=
|
|
|
ENST00000682178.1:n.2174G=
|
|
|
ENST00000682345.1:c.*842G=
|
ENSP00000508122.1:n.*842G=
|
|
ENST00000682452.1:n.1473G=
|
|
|
ENST00000682456.1:c.1001G=
|
ENSP00000508240.1:p.Gly334=
|
|
ENST00000682566.1:n.1925G=
|
|
|
ENST00000682613.1:n.1454G=
|
|
|
ENST00000682734.1:c.-32G=
|
ENSP00000507860.1:n.-32G=
|
|
ENST00000682820.1:n.1179G=
|
|
|
ENST00000683004.1:c.*835G=
|
ENSP00000506936.1:n.*835G=
|
|
ENST00000683079.1:c.*567G=
|
ENSP00000507296.1:n.*567G=
|
|
ENST00000683081.1:c.*979G=
|
ENSP00000507722.1:n.*979G=
|
|
ENST00000683181.1:n.421G=
|
|
|
ENST00000683209.1:n.3468G=
|
|
|
ENST00000683305.1:c.959G=
|
ENSP00000508043.1:p.Gly320=
|
|
ENST00000683448.1:c.*62G=
|
ENSP00000506931.1:n.*62G=
|
|
ENST00000683478.1:c.*493G=
|
ENSP00000507793.1:n.*493G=
|
|
ENST00000683483.1:c.998G=
|
ENSP00000507719.1:p.Gly333=
|
|
ENST00000683622.1:n.856G=
|
|
|
ENST00000683751.1:c.647G=
|
ENSP00000506944.1:p.Gly216=
|
|
ENST00000684036.1:c.959G=
|
ENSP00000507276.1:p.Gly320=
|
|
ENST00000684129.1:c.-32G=
|
ENSP00000507174.1:n.-32G=
|
|
ENST00000684209.1:n.1517G=
|
|
|
ENST00000684296.1:c.*62G=
|
ENSP00000507740.1:n.*62G=
|
|
ENST00000684505.1:c.1091G=
|
ENSP00000508237.1:p.Gly364=
|
|
ENST00000684552.1:c.*62G=
|
ENSP00000506899.1:n.*62G=
|
|
ENST00000684611.1:n.2870G=
|
|
|
ENST00000684622.1:c.1142G=
|
ENSP00000507546.1:p.Gly381=
|
|
ENST00000684627.1:c.959G=
|
ENSP00000507471.1:p.Gly320=
|
|
ENST00000684641.1:c.857G=
|
ENSP00000507642.1:p.Gly286=
|
|
ENST00000684675.1:c.1183G=
|
ENSP00000506934.1:p.Val395=
|
|
ENST00000684749.1:n.1211G=
|
|
|
ENST00000511912.6:c.1142G=
MANE Select
|
ENSP00000426638.1:p.Gly381=
|
|
ENST00000307738.5:c.1001G=
|
ENSP00000303552.5:p.Gly334=
|
|
ENST00000506422.1:n.112G=
|
|
|
ENST00000511912.5:c.1142G=
|
ENSP00000426638.1:p.Gly381=
|
|
NM_001281737.1:c.1001G=
|
NP_001268666.1:p.Gly334=
|
|
NM_001281738.1:c.959G=
|
NP_001268667.1:p.Gly320=
|
|
NM_004453.3:c.1142G=
|
NP_004444.2:p.Gly381=
|
|
XM_024453935.1:c.959G=
|
XP_024309703.1:p.Gly320=
|
|
NM_004453.4:c.1142G=
MANE Select
|
NP_004444.2:p.Gly381=
|
|
NM_001281737.2:c.1001G=
|
NP_001268666.1:p.Gly334=
|
|