ENST00000269980.7:c.234C>G
MANE Select
|
ENSP00000269980.2:p.Ile78Met
|
|
ENST00000269980.6:c.234C>G
|
ENSP00000269980.2:p.Ile78Met
|
|
ENST00000457836.6:c.168C>G
|
ENSP00000416000.2:p.Ile56Met
|
|
ENST00000538423.5:n.254C>G
|
|
|
ENST00000540732.3:c.336C>G
|
ENSP00000443246.1:p.Ile112Met
|
|
ENST00000541315.1:c.41C>G
|
|
|
ENST00000542943.5:c.234C>G
|
ENSP00000440345.1:p.Ile78Met
|
|
ENST00000595085.5:c.234C>G
|
ENSP00000471150.2:p.Ile78Met
|
|
ENST00000604424.1:n.476C>G
|
|
|
NM_000709.3:c.234C>G
|
NP_000700.1:p.Ile78Met
|
|
NM_001164783.1:c.234C>G
|
NP_001158255.1:p.Ile78Met
|
|
NM_000709.4:c.234C>G
MANE Select
|
NP_000700.1:p.Ile78Met
|
|
NM_001164783.2:c.234C>G
|
NP_001158255.1:p.Ile78Met
|
|