ENST00000269980.7:c.880A>G
MANE Select
|
ENSP00000269980.2:p.Met294Val
|
|
ENST00000269980.6:c.880A>G
|
ENSP00000269980.2:p.Met294Val
|
|
ENST00000457836.6:c.814A>G
|
ENSP00000416000.2:p.Met272Val
|
|
ENST00000535632.5:n.509A>G
|
|
|
ENST00000540732.3:c.982A>G
|
ENSP00000443246.1:p.Met328Val
|
|
ENST00000542943.5:c.793A>G
|
ENSP00000440345.1:p.Met265Val
|
|
ENST00000545787.1:n.508A>G
|
|
|
ENST00000595085.5:c.880A>G
|
ENSP00000471150.2:p.Met294Val
|
|
NM_000709.3:c.880A>G
|
NP_000700.1:p.Met294Val
|
|
NM_001164783.1:c.877A>G
|
NP_001158255.1:p.Met293Val
|
|
NM_000709.4:c.880A>G
MANE Select
|
NP_000700.1:p.Met294Val
|
|
NM_001164783.2:c.877A>G
|
NP_001158255.1:p.Met293Val
|
|