ENST00000398603.6:c.337A>G
|
ENSP00000381604.1:p.Ile113Val
|
|
ENST00000398606.10:c.445A>G
MANE Select
|
ENSP00000381607.3:p.Ile149Val
|
|
ENST00000646888.1:c.*161A>G
|
ENSP00000494477.1:n.*161A>G
|
|
ENST00000398603.5:c.337A>G
|
ENSP00000381604.1:p.Ile113Val
|
|
ENST00000398606.7:c.445A>G
|
ENSP00000381607.3:p.Ile149Val
|
|
ENST00000467591.1:n.556A>G
|
|
|
ENST00000494593.1:n.1417A>G
|
|
|
ENST00000495996.1:c.171A>G
|
ENSP00000484686.1:p.Val57=
|
|
ENST00000498765.5:c.508A>G
|
|
|
NM_000852.3:c.445A>G , LRG_723t1:c.445A>G
|
NP_000843.1:p.Ile149Val
|
|
NM_000852.4:c.445A>G
MANE Select
|
NP_000843.1:p.Ile149Val
|
|