ENST00000269980.7:c.286C>A
MANE Select
|
ENSP00000269980.2:p.His96Asn
|
|
ENST00000269980.6:c.286C>A
|
ENSP00000269980.2:p.His96Asn
|
|
ENST00000457836.6:c.220C>A
|
ENSP00000416000.2:p.His74Asn
|
|
ENST00000538423.5:n.306C>A
|
|
|
ENST00000540732.3:c.388C>A
|
ENSP00000443246.1:p.His130Asn
|
|
ENST00000541315.1:c.93C>A
|
|
|
ENST00000542943.5:c.286C>A
|
ENSP00000440345.1:p.His96Asn
|
|
ENST00000595085.5:c.286C>A
|
ENSP00000471150.2:p.His96Asn
|
|
ENST00000604424.1:n.528C>A
|
|
|
NM_000709.3:c.286C>A
|
NP_000700.1:p.His96Asn
|
|
NM_001164783.1:c.286C>A
|
NP_001158255.1:p.His96Asn
|
|
NM_000709.4:c.286C>A
MANE Select
|
NP_000700.1:p.His96Asn
|
|
NM_001164783.2:c.286C>A
|
NP_001158255.1:p.His96Asn
|
|