ENST00000269980.7:c.1254C>G
MANE Select
|
ENSP00000269980.2:p.Ala418=
|
|
ENST00000269980.6:c.1254C>G
|
ENSP00000269980.2:p.Ala418=
|
|
ENST00000457836.6:c.1263C>G
|
ENSP00000416000.2:p.Ala421=
|
|
ENST00000540732.3:c.1356C>G
|
ENSP00000443246.1:p.Ala452=
|
|
ENST00000544905.1:c.84C>G
|
|
|
ENST00000595085.5:c.922+1827C>G
|
ENSP00000471150.2:n.922+1827C>G
|
|
NM_000709.3:c.1254C>G
|
NP_000700.1:p.Ala418=
|
|
NM_001164783.1:c.1251C>G
|
NP_001158255.1:p.Ala417=
|
|
NM_000709.4:c.1254C>G
MANE Select
|
NP_000700.1:p.Ala418=
|
|
NM_001164783.2:c.1251C>G
|
NP_001158255.1:p.Ala417=
|
|