ENST00000269980.7:c.1196G=
MANE Select
|
ENSP00000269980.2:p.Arg399=
|
|
ENST00000269980.6:c.1196G=
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ENSP00000269980.2:p.Arg399=
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|
ENST00000457836.6:c.1205G=
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ENSP00000416000.2:p.Arg402=
|
|
ENST00000540732.3:c.1298G=
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ENSP00000443246.1:p.Arg433=
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|
ENST00000544905.1:c.62-36G=
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|
|
ENST00000595085.5:c.922+1769G=
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ENSP00000471150.2:n.922+1769G=
|
|
NM_000709.3:c.1196G=
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NP_000700.1:p.Arg399=
|
|
NM_001164783.1:c.1193G=
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NP_001158255.1:p.Arg398=
|
|
NM_000709.4:c.1196G=
MANE Select
|
NP_000700.1:p.Arg399=
|
|
NM_001164783.2:c.1193G=
|
NP_001158255.1:p.Arg398=
|
|