ENST00000330062.8:c.503T>G
MANE Select
|
ENSP00000331897.4:p.Ile168Ser
|
|
ENST00000330062.7:c.503T>G
|
ENSP00000331897.3:p.Ile168Ser
|
|
ENST00000540499.2:c.347T>G
|
ENSP00000446147.2:p.Ile116Ser
|
|
ENST00000559482.5:c.208-116T>G
|
ENSP00000453016.1:n.208-116T>G
|
|
ENST00000560061.1:c.*128T>G
|
ENSP00000453254.1:n.*128T>G
|
|
NM_001289910.1:c.347T>G , LRG_611t1:c.347T>G
|
NP_001276839.1:p.Ile116Ser
|
|
NM_001290114.1:c.113T>G
|
NP_001277043.1:p.Ile38Ser
|
|
NM_002168.3:c.503T>G , LRG_611t2:c.503T>G
|
NP_002159.2:p.Ile168Ser
|
|
NM_001290114.2:c.113T>G
|
NP_001277043.1:p.Ile38Ser
|
|
NM_002168.4:c.503T>G
MANE Select
|
NP_002159.2:p.Ile168Ser
|
|