ENST00000398603.6:c.337-195T>G
|
ENSP00000381604.1:n.337-195T>G
|
|
ENST00000398606.10:c.427T>G
MANE Select
|
ENSP00000381607.3:p.Phe143Val
|
|
ENST00000646888.1:c.*143T>G
|
ENSP00000494477.1:n.*143T>G
|
|
ENST00000398603.5:c.337-195T>G
|
ENSP00000381604.1:n.337-195T>G
|
|
ENST00000398606.7:c.427T>G
|
ENSP00000381607.3:p.Phe143Val
|
|
ENST00000467591.1:n.538T>G
|
|
|
ENST00000494593.1:n.1222T>G
|
|
|
ENST00000495996.1:c.91T>G
|
ENSP00000484686.1:p.Phe31Val
|
|
ENST00000498765.5:c.490T>G
|
|
|
NM_000852.3:c.427T>G , LRG_723t1:c.427T>G
|
NP_000843.1:p.Phe143Val
|
|
NM_000852.4:c.427T>G
MANE Select
|
NP_000843.1:p.Phe143Val
|
|