ENST00000496887.7:c.556C>G
|
ENSP00000434560.2:p.Leu186Val
|
|
ENST00000646564.2:c.478-10553C>G
|
ENSP00000495806.2:n.478-10553C>G
|
|
ENST00000155840.12:c.817C>G
MANE Select
|
ENSP00000155840.2:p.Leu273Val
|
|
ENST00000335475.6:c.436C>G
|
ENSP00000334497.5:p.Leu146Val
|
|
ENST00000646564.1:c.124-10553C>G
|
ENSP00000495806.1:n.124-10553C>G
|
|
ENST00000155840.9:c.817C>G
|
ENSP00000155840.2:p.Leu273Val
|
|
ENST00000335475.5:c.436C>G
|
ENSP00000334497.5:p.Leu146Val
|
|
ENST00000496887.6:c.556C>G
|
ENSP00000434560.1:p.Leu186Val
|
|
NM_000218.2:c.817C>G , LRG_287t1:c.817C>G
|
NP_000209.2:p.Leu273Val
|
|
NM_181798.1:c.436C>G , LRG_287t2:c.436C>G
|
NP_861463.1:p.Leu146Val
|
|
NM_000218.3:c.817C>G
MANE Select
|
NP_000209.2:p.Leu273Val
|
|