ENST00000398603.6:c.337-268C>G
|
ENSP00000381604.1:n.337-268C>G
|
|
ENST00000398606.10:c.354C>G
MANE Select
|
ENSP00000381607.3:p.Asp118Glu
|
|
ENST00000646888.1:c.*70C>G
|
ENSP00000494477.1:n.*70C>G
|
|
ENST00000398603.5:c.337-268C>G
|
ENSP00000381604.1:n.337-268C>G
|
|
ENST00000398606.7:c.354C>G
|
ENSP00000381607.3:p.Asp118Glu
|
|
ENST00000467591.1:n.465C>G
|
|
|
ENST00000494593.1:n.1149C>G
|
|
|
ENST00000495996.1:c.18C>G
|
ENSP00000484686.1:p.Asp6Glu
|
|
ENST00000498765.5:c.417C>G
|
|
|
NM_000852.3:c.354C>G , LRG_723t1:c.354C>G
|
NP_000843.1:p.Asp118Glu
|
|
NM_000852.4:c.354C>G
MANE Select
|
NP_000843.1:p.Asp118Glu
|
|