ENST00000269980.7:c.818C>G
MANE Select
|
ENSP00000269980.2:p.Thr273Arg
|
|
ENST00000269980.6:c.818C>G
|
ENSP00000269980.2:p.Thr273Arg
|
|
ENST00000457836.6:c.752C>G
|
ENSP00000416000.2:p.Thr251Arg
|
|
ENST00000535632.5:n.447C>G
|
|
|
ENST00000540732.3:c.920C>G
|
ENSP00000443246.1:p.Thr307Arg
|
|
ENST00000542943.5:c.731C>G
|
ENSP00000440345.1:p.Thr244Arg
|
|
ENST00000545787.1:n.446C>G
|
|
|
ENST00000595085.5:c.818C>G
|
ENSP00000471150.2:p.Thr273Arg
|
|
NM_000709.3:c.818C>G
|
NP_000700.1:p.Thr273Arg
|
|
NM_001164783.1:c.818C>G
|
NP_001158255.1:p.Thr273Arg
|
|
NM_000709.4:c.818C>G
MANE Select
|
NP_000700.1:p.Thr273Arg
|
|
NM_001164783.2:c.818C>G
|
NP_001158255.1:p.Thr273Arg
|
|