ENST00000269980.7:c.1310A=
MANE Select
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ENSP00000269980.2:p.His437=
|
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ENST00000269980.6:c.1310A=
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ENSP00000269980.2:p.His437=
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|
ENST00000457836.6:c.1319A=
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ENSP00000416000.2:p.His440=
|
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ENST00000540732.3:c.1412A=
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ENSP00000443246.1:p.His471=
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ENST00000544905.1:c.140A=
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|
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ENST00000595085.5:c.922+1883A=
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ENSP00000471150.2:n.922+1883A=
|
|
NM_000709.3:c.1310A=
|
NP_000700.1:p.His437=
|
|
NM_001164783.1:c.1307A=
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NP_001158255.1:p.His436=
|
|
NM_000709.4:c.1310A=
MANE Select
|
NP_000700.1:p.His437=
|
|
NM_001164783.2:c.1307A=
|
NP_001158255.1:p.His436=
|
|