ENST00000269980.7:c.1286G=
MANE Select
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ENSP00000269980.2:p.Arg429=
|
|
ENST00000269980.6:c.1286G=
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ENSP00000269980.2:p.Arg429=
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|
ENST00000457836.6:c.1295G=
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ENSP00000416000.2:p.Arg432=
|
|
ENST00000540732.3:c.1388G=
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ENSP00000443246.1:p.Arg463=
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ENST00000544905.1:c.116G=
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|
|
ENST00000595085.5:c.922+1859G=
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ENSP00000471150.2:n.922+1859G=
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|
NM_000709.3:c.1286G=
|
NP_000700.1:p.Arg429=
|
|
NM_001164783.1:c.1283G=
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NP_001158255.1:p.Arg428=
|
|
NM_000709.4:c.1286G=
MANE Select
|
NP_000700.1:p.Arg429=
|
|
NM_001164783.2:c.1283G=
|
NP_001158255.1:p.Arg428=
|
|