ENST00000269980.7:c.1031C>G
MANE Select
|
ENSP00000269980.2:p.Ala344Gly
|
|
ENST00000269980.6:c.1031C>G
|
ENSP00000269980.2:p.Ala344Gly
|
|
ENST00000457836.6:c.1040C>G
|
ENSP00000416000.2:p.Ala347Gly
|
|
ENST00000540732.3:c.1133C>G
|
ENSP00000443246.1:p.Ala378Gly
|
|
ENST00000542943.5:c.944C>G
|
ENSP00000440345.1:p.Ala315Gly
|
|
ENST00000595085.5:c.922+336C>G
|
ENSP00000471150.2:n.922+336C>G
|
|
NM_000709.3:c.1031C>G
|
NP_000700.1:p.Ala344Gly
|
|
NM_001164783.1:c.1028C>G
|
NP_001158255.1:p.Ala343Gly
|
|
NM_000709.4:c.1031C>G
MANE Select
|
NP_000700.1:p.Ala344Gly
|
|
NM_001164783.2:c.1028C>G
|
NP_001158255.1:p.Ala343Gly
|
|