ENST00000398603.6:c.369G>A
|
ENSP00000381604.1:p.Leu123=
|
|
ENST00000398606.10:c.477G>A
MANE Select
|
ENSP00000381607.3:p.Leu159=
|
|
ENST00000646888.1:c.*193G>A
|
ENSP00000494477.1:n.*193G>A
|
|
ENST00000398603.5:c.369G>A
|
ENSP00000381604.1:p.Leu123=
|
|
ENST00000398606.7:c.477G>A
|
ENSP00000381607.3:p.Leu159=
|
|
ENST00000467591.1:n.588G>A
|
|
|
ENST00000494593.1:n.1449G>A
|
|
|
ENST00000495996.1:c.203G>A
|
ENSP00000484686.1:p.Cys68Tyr
|
|
ENST00000498765.5:c.540G>A
|
|
|
NM_000852.3:c.477G>A , LRG_723t1:c.477G>A
|
NP_000843.1:p.Leu159=
|
|
NM_000852.4:c.477G>A
MANE Select
|
NP_000843.1:p.Leu159=
|
|