ENST00000367435.5:c.1004C>A
MANE Select
|
ENSP00000356405.4:p.Pro335His
|
|
ENST00000635846.1:c.761C>A
|
ENSP00000490035.1:p.Pro254His
|
|
ENST00000643006.1:c.1072C>A
|
ENSP00000496633.1:p.Leu358Met
|
|
ENST00000648071.1:c.*980C>A
|
ENSP00000497513.1:n.*980C>A
|
|
ENST00000649613.1:n.254C>A
|
|
|
ENST00000649895.1:n.1222C>A
|
|
|
ENST00000650197.1:c.1004C>A
|
ENSP00000496929.1:p.Pro335His
|
|
ENST00000367435.3:c.1004C>A
|
ENSP00000356405.3:p.Pro335His
|
|
NM_024529.4:c.1004C>A , LRG_507t1:c.1004C>A
|
NP_078805.3:p.Pro335His
|
|
NM_024529.5:c.1004C>A
MANE Select
|
NP_078805.3:p.Pro335His
|
|