ENST00000269980.7:c.1274A>C
MANE Select
|
ENSP00000269980.2:p.Glu425Ala
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ENST00000269980.6:c.1274A>C
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ENSP00000269980.2:p.Glu425Ala
|
|
ENST00000457836.6:c.1283A>C
|
ENSP00000416000.2:p.Glu428Ala
|
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ENST00000540732.3:c.1376A>C
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ENSP00000443246.1:p.Glu459Ala
|
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ENST00000544905.1:c.104A>C
|
|
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ENST00000595085.5:c.922+1847A>C
|
ENSP00000471150.2:n.922+1847A>C
|
|
NM_000709.3:c.1274A>C
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NP_000700.1:p.Glu425Ala
|
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NM_001164783.1:c.1271A>C
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NP_001158255.1:p.Glu424Ala
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|
NM_000709.4:c.1274A>C
MANE Select
|
NP_000700.1:p.Glu425Ala
|
|
NM_001164783.2:c.1271A>C
|
NP_001158255.1:p.Glu424Ala
|
|