ENST00000398603.6:c.434T>A
|
ENSP00000381604.1:p.Val145Glu
|
|
ENST00000398606.10:c.542T>A
MANE Select
|
ENSP00000381607.3:p.Val181Glu
|
|
ENST00000646888.1:c.*258T>A
|
ENSP00000494477.1:n.*258T>A
|
|
ENST00000398603.5:c.434T>A
|
ENSP00000381604.1:p.Val145Glu
|
|
ENST00000398606.7:c.542T>A
|
ENSP00000381607.3:p.Val181Glu
|
|
ENST00000467591.1:n.653T>A
|
|
|
ENST00000494593.1:n.1514T>A
|
|
|
ENST00000498765.5:c.605T>A
|
|
|
NM_000852.3:c.542T>A , LRG_723t1:c.542T>A
|
NP_000843.1:p.Val181Glu
|
|
NM_000852.4:c.542T>A
MANE Select
|
NP_000843.1:p.Val181Glu
|
|