ENST00000269980.7:c.367C>T
MANE Select
|
ENSP00000269980.2:p.Gln123Ter
|
|
ENST00000269980.6:c.367C>T
|
ENSP00000269980.2:p.Gln123Ter
|
|
ENST00000457836.6:c.301C>T
|
ENSP00000416000.2:p.Gln101Ter
|
|
ENST00000538423.5:n.493C>T
|
|
|
ENST00000540732.3:c.469C>T
|
ENSP00000443246.1:p.Gln157Ter
|
|
ENST00000541315.1:c.174C>T
|
|
|
ENST00000542943.5:c.288+185C>T
|
ENSP00000440345.1:n.288+185C>T
|
|
ENST00000595085.5:c.367C>T
|
ENSP00000471150.2:p.Gln123Ter
|
|
NM_000709.3:c.367C>T
|
NP_000700.1:p.Gln123Ter
|
|
NM_001164783.1:c.367C>T
|
NP_001158255.1:p.Gln123Ter
|
|
NM_000709.4:c.367C>T
MANE Select
|
NP_000700.1:p.Gln123Ter
|
|
NM_001164783.2:c.367C>T
|
NP_001158255.1:p.Gln123Ter
|
|