ENST00000367435.5:c.1022C>G
MANE Select
|
ENSP00000356405.4:p.Pro341Arg
|
|
ENST00000635846.1:c.779C>G
|
ENSP00000490035.1:p.Pro260Arg
|
|
ENST00000643006.1:c.1090C>G
|
ENSP00000496633.1:p.Gln364Glu
|
|
ENST00000648071.1:c.*998C>G
|
ENSP00000497513.1:n.*998C>G
|
|
ENST00000649613.1:n.272C>G
|
|
|
ENST00000649895.1:n.1240C>G
|
|
|
ENST00000650197.1:c.1022C>G
|
ENSP00000496929.1:p.Pro341Arg
|
|
ENST00000367435.3:c.1022C>G
|
ENSP00000356405.3:p.Pro341Arg
|
|
NM_024529.4:c.1022C>G , LRG_507t1:c.1022C>G
|
NP_078805.3:p.Pro341Arg
|
|
NM_024529.5:c.1022C>G
MANE Select
|
NP_078805.3:p.Pro341Arg
|
|