ENST00000398603.6:c.421C>G
|
ENSP00000381604.1:p.Leu141Val
|
|
ENST00000398606.10:c.529C>G
MANE Select
|
ENSP00000381607.3:p.Leu177Val
|
|
ENST00000646888.1:c.*245C>G
|
ENSP00000494477.1:n.*245C>G
|
|
ENST00000398603.5:c.421C>G
|
ENSP00000381604.1:p.Leu141Val
|
|
ENST00000398606.7:c.529C>G
|
ENSP00000381607.3:p.Leu177Val
|
|
ENST00000467591.1:n.640C>G
|
|
|
ENST00000494593.1:n.1501C>G
|
|
|
ENST00000498765.5:c.592C>G
|
|
|
NM_000852.3:c.529C>G , LRG_723t1:c.529C>G
|
NP_000843.1:p.Leu177Val
|
|
NM_000852.4:c.529C>G
MANE Select
|
NP_000843.1:p.Leu177Val
|
|