ENST00000269980.7:c.1008C=
MANE Select
|
ENSP00000269980.2:p.His336=
|
|
ENST00000269980.6:c.1008C=
|
ENSP00000269980.2:p.His336=
|
|
ENST00000457836.6:c.1017C=
|
ENSP00000416000.2:p.His339=
|
|
ENST00000540732.3:c.1110C=
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ENSP00000443246.1:p.His370=
|
|
ENST00000542943.5:c.921C=
|
ENSP00000440345.1:p.His307=
|
|
ENST00000595085.5:c.922+313C=
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ENSP00000471150.2:n.922+313C=
|
|
NM_000709.3:c.1008C=
|
NP_000700.1:p.His336=
|
|
NM_001164783.1:c.1005C=
|
NP_001158255.1:p.His335=
|
|
NM_000709.4:c.1008C=
MANE Select
|
NP_000700.1:p.His336=
|
|
NM_001164783.2:c.1005C=
|
NP_001158255.1:p.His335=
|
|