ENST00000269980.7:c.1246A=
MANE Select
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ENSP00000269980.2:p.Met416=
|
|
ENST00000269980.6:c.1246A=
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ENSP00000269980.2:p.Met416=
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ENST00000457836.6:c.1255A=
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ENSP00000416000.2:p.Met419=
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ENST00000540732.3:c.1348A=
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ENSP00000443246.1:p.Met450=
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ENST00000544905.1:c.76A=
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|
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ENST00000595085.5:c.922+1819A=
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ENSP00000471150.2:n.922+1819A=
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|
NM_000709.3:c.1246A=
|
NP_000700.1:p.Met416=
|
|
NM_001164783.1:c.1243A=
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NP_001158255.1:p.Met415=
|
|
NM_000709.4:c.1246A=
MANE Select
|
NP_000700.1:p.Met416=
|
|
NM_001164783.2:c.1243A=
|
NP_001158255.1:p.Met415=
|
|