ENST00000398603.6:c.337-215A>G
|
ENSP00000381604.1:n.337-215A>G
|
|
ENST00000398606.10:c.407A>G
MANE Select
|
ENSP00000381607.3:p.Gln136Arg
|
|
ENST00000646888.1:c.*123A>G
|
ENSP00000494477.1:n.*123A>G
|
|
ENST00000398603.5:c.337-215A>G
|
ENSP00000381604.1:n.337-215A>G
|
|
ENST00000398606.7:c.407A>G
|
ENSP00000381607.3:p.Gln136Arg
|
|
ENST00000467591.1:n.518A>G
|
|
|
ENST00000494593.1:n.1202A>G
|
|
|
ENST00000495996.1:c.71A>G
|
ENSP00000484686.1:p.Gln24Arg
|
|
ENST00000498765.5:c.470A>G
|
|
|
NM_000852.3:c.407A>G , LRG_723t1:c.407A>G
|
NP_000843.1:p.Gln136Arg
|
|
NM_000852.4:c.407A>G
MANE Select
|
NP_000843.1:p.Gln136Arg
|
|