ENST00000398603.6:c.337-283G>A
|
ENSP00000381604.1:n.337-283G>A
|
|
ENST00000398606.10:c.339G>A
MANE Select
|
ENSP00000381607.3:p.Glu113=
|
|
ENST00000646888.1:c.*55G>A
|
ENSP00000494477.1:n.*55G>A
|
|
ENST00000398603.5:c.337-283G>A
|
ENSP00000381604.1:n.337-283G>A
|
|
ENST00000398606.7:c.339G>A
|
ENSP00000381607.3:p.Glu113=
|
|
ENST00000467591.1:n.450G>A
|
|
|
ENST00000494593.1:n.1134G>A
|
|
|
ENST00000495996.1:c.3G>A
|
ENSP00000484686.1:p.Glu1=
|
|
ENST00000498765.5:c.402G>A
|
|
|
NM_000852.3:c.339G>A , LRG_723t1:c.339G>A
|
NP_000843.1:p.Glu113=
|
|
NM_000852.4:c.339G>A
MANE Select
|
NP_000843.1:p.Glu113=
|
|