ENST00000330062.8:c.375G>C
MANE Select
|
ENSP00000331897.4:p.Glu125Asp
|
|
ENST00000330062.7:c.375G>C
|
ENSP00000331897.3:p.Glu125Asp
|
|
ENST00000540499.2:c.219G>C
|
ENSP00000446147.2:p.Glu73Asp
|
|
ENST00000559482.5:c.208-244G>C
|
ENSP00000453016.1:n.208-244G>C
|
|
ENST00000560061.1:c.117G>C
|
ENSP00000453254.1:p.Ter39Tyr
|
|
NM_001289910.1:c.219G>C , LRG_611t1:c.219G>C
|
NP_001276839.1:p.Glu73Asp
|
|
NM_001290114.1:c.-16G>C
|
NP_001277043.1:n.-16G>C
|
|
NM_002168.3:c.375G>C , LRG_611t2:c.375G>C
|
NP_002159.2:p.Glu125Asp
|
|
NM_001290114.2:c.-16G>C
|
NP_001277043.1:n.-16G>C
|
|
NM_002168.4:c.375G>C
MANE Select
|
NP_002159.2:p.Glu125Asp
|
|