ENST00000269980.7:c.360T>C
MANE Select
|
ENSP00000269980.2:p.Tyr120=
|
|
ENST00000269980.6:c.360T>C
|
ENSP00000269980.2:p.Tyr120=
|
|
ENST00000457836.6:c.294T>C
|
ENSP00000416000.2:p.Tyr98=
|
|
ENST00000538423.5:n.486T>C
|
|
|
ENST00000540732.3:c.462T>C
|
ENSP00000443246.1:p.Tyr154=
|
|
ENST00000541315.1:c.167T>C
|
|
|
ENST00000542943.5:c.288+178T>C
|
ENSP00000440345.1:n.288+178T>C
|
|
ENST00000595085.5:c.360T>C
|
ENSP00000471150.2:p.Tyr120=
|
|
NM_000709.3:c.360T>C
|
NP_000700.1:p.Tyr120=
|
|
NM_001164783.1:c.360T>C
|
NP_001158255.1:p.Tyr120=
|
|
NM_000709.4:c.360T>C
MANE Select
|
NP_000700.1:p.Tyr120=
|
|
NM_001164783.2:c.360T>C
|
NP_001158255.1:p.Tyr120=
|
|