ENST00000370263.9:c.514C>G
MANE Select
|
ENSP00000359285.4:p.Gln172Glu
|
|
ENST00000370263.8:c.514C>G
|
ENSP00000359285.4:p.Gln172Glu
|
|
ENST00000463705.5:n.1162C>G
|
|
|
ENST00000467563.3:n.584C>G
|
|
|
ENST00000498043.6:c.538C>G
|
|
|
ENST00000615287.4:c.301C>G
|
ENSP00000483388.1:p.Gln101Glu
|
|
ENST00000627000.1:c.*203C>G
|
ENSP00000486914.1:n.*203C>G
|
|
ENST00000630240.1:n.235C>G
|
|
|
NM_000744.6:c.514C>G
|
NP_000735.1:p.Gln172Glu
|
|
NM_001256573.1:c.-15C>G
|
NP_001243502.1:n.-15C>G
|
|
NR_046317.1:n.770C>G
|
|
|
XM_011528524.1:c.301C>G
|
XP_011526826.1:p.Gln101Glu
|
|
XM_017027625.2:c.-15C>G
|
XP_016883114.1:n.-15C>G
|
|
XM_024451822.1:c.-15C>G
|
XP_024307590.1:n.-15C>G
|
|
NM_001256573.2:c.-15C>G
|
NP_001243502.1:n.-15C>G
|
|
NR_046317.2:n.723C>G
|
|
|
NM_000744.7:c.514C>G
MANE Select
|
NP_000735.1:p.Gln172Glu
|
|