ENST00000269980.7:c.1031C>T
MANE Select
|
ENSP00000269980.2:p.Ala344Val
|
|
ENST00000269980.6:c.1031C>T
|
ENSP00000269980.2:p.Ala344Val
|
|
ENST00000457836.6:c.1040C>T
|
ENSP00000416000.2:p.Ala347Val
|
|
ENST00000540732.3:c.1133C>T
|
ENSP00000443246.1:p.Ala378Val
|
|
ENST00000542943.5:c.944C>T
|
ENSP00000440345.1:p.Ala315Val
|
|
ENST00000595085.5:c.922+336C>T
|
ENSP00000471150.2:n.922+336C>T
|
|
NM_000709.3:c.1031C>T
|
NP_000700.1:p.Ala344Val
|
|
NM_001164783.1:c.1028C>T
|
NP_001158255.1:p.Ala343Val
|
|
NM_000709.4:c.1031C>T
MANE Select
|
NP_000700.1:p.Ala344Val
|
|
NM_001164783.2:c.1028C>T
|
NP_001158255.1:p.Ala343Val
|
|