ENST00000398603.6:c.338T>G
|
ENSP00000381604.1:p.Ile113Ser
|
|
ENST00000398606.10:c.446T>G
MANE Select
|
ENSP00000381607.3:p.Ile149Ser
|
|
ENST00000646888.1:c.*162T>G
|
ENSP00000494477.1:n.*162T>G
|
|
ENST00000398603.5:c.338T>G
|
ENSP00000381604.1:p.Ile113Ser
|
|
ENST00000398606.7:c.446T>G
|
ENSP00000381607.3:p.Ile149Ser
|
|
ENST00000467591.1:n.557T>G
|
|
|
ENST00000494593.1:n.1418T>G
|
|
|
ENST00000495996.1:c.172T>G
|
ENSP00000484686.1:p.Ser58Ala
|
|
ENST00000498765.5:c.509T>G
|
|
|
NM_000852.3:c.446T>G , LRG_723t1:c.446T>G
|
NP_000843.1:p.Ile149Ser
|
|
NM_000852.4:c.446T>G
MANE Select
|
NP_000843.1:p.Ile149Ser
|
|