ENST00000398603.6:c.361C>G
|
ENSP00000381604.1:p.Leu121Val
|
|
ENST00000398606.10:c.469C>G
MANE Select
|
ENSP00000381607.3:p.Leu157Val
|
|
ENST00000646888.1:c.*185C>G
|
ENSP00000494477.1:n.*185C>G
|
|
ENST00000398603.5:c.361C>G
|
ENSP00000381604.1:p.Leu121Val
|
|
ENST00000398606.7:c.469C>G
|
ENSP00000381607.3:p.Leu157Val
|
|
ENST00000467591.1:n.580C>G
|
|
|
ENST00000494593.1:n.1441C>G
|
|
|
ENST00000495996.1:c.195C>G
|
ENSP00000484686.1:p.Cys65Trp
|
|
ENST00000498765.5:c.532C>G
|
|
|
NM_000852.3:c.469C>G , LRG_723t1:c.469C>G
|
NP_000843.1:p.Leu157Val
|
|
NM_000852.4:c.469C>G
MANE Select
|
NP_000843.1:p.Leu157Val
|
|