ENST00000367435.5:c.1494A>C
MANE Select
|
ENSP00000356405.4:p.Glu498Asp
|
|
ENST00000635846.1:c.1251A>C
|
ENSP00000490035.1:p.Glu417Asp
|
|
ENST00000643006.1:c.*404A>C
|
ENSP00000496633.1:n.*404A>C
|
|
ENST00000648071.1:c.*1470A>C
|
ENSP00000497513.1:n.*1470A>C
|
|
ENST00000649613.1:n.744A>C
|
|
|
ENST00000650197.1:c.*192A>C
|
ENSP00000496929.1:n.*192A>C
|
|
ENST00000367435.3:c.1494A>C
|
ENSP00000356405.3:p.Glu498Asp
|
|
ENST00000477868.1:n.206A>C
|
|
|
NM_024529.4:c.1494A>C , LRG_507t1:c.1494A>C
|
NP_078805.3:p.Glu498Asp
|
|
NM_024529.5:c.1494A>C
MANE Select
|
NP_078805.3:p.Glu498Asp
|
|