ENST00000398603.6:c.410C>T
|
ENSP00000381604.1:p.Ala137Val
|
|
ENST00000398606.10:c.518C>T
MANE Select
|
ENSP00000381607.3:p.Ala173Val
|
|
ENST00000646888.1:c.*234C>T
|
ENSP00000494477.1:n.*234C>T
|
|
ENST00000398603.5:c.410C>T
|
ENSP00000381604.1:p.Ala137Val
|
|
ENST00000398606.7:c.518C>T
|
ENSP00000381607.3:p.Ala173Val
|
|
ENST00000467591.1:n.629C>T
|
|
|
ENST00000494593.1:n.1490C>T
|
|
|
ENST00000498765.5:c.581C>T
|
|
|
NM_000852.3:c.518C>T , LRG_723t1:c.518C>T
|
NP_000843.1:p.Ala173Val
|
|
NM_000852.4:c.518C>T
MANE Select
|
NP_000843.1:p.Ala173Val
|
|