ENST00000398603.6:c.337-241G>A
|
ENSP00000381604.1:n.337-241G>A
|
|
ENST00000398606.10:c.381G>A
MANE Select
|
ENSP00000381607.3:p.Leu127=
|
|
ENST00000646888.1:c.*97G>A
|
ENSP00000494477.1:n.*97G>A
|
|
ENST00000398603.5:c.337-241G>A
|
ENSP00000381604.1:n.337-241G>A
|
|
ENST00000398606.7:c.381G>A
|
ENSP00000381607.3:p.Leu127=
|
|
ENST00000467591.1:n.492G>A
|
|
|
ENST00000494593.1:n.1176G>A
|
|
|
ENST00000495996.1:c.45G>A
|
ENSP00000484686.1:p.Leu15=
|
|
ENST00000498765.5:c.444G>A
|
|
|
NM_000852.3:c.381G>A , LRG_723t1:c.381G>A
|
NP_000843.1:p.Leu127=
|
|
NM_000852.4:c.381G>A
MANE Select
|
NP_000843.1:p.Leu127=
|
|