ENST00000269980.7:c.1284C>T
MANE Select
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ENSP00000269980.2:p.Ala428=
|
|
ENST00000269980.6:c.1284C>T
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ENSP00000269980.2:p.Ala428=
|
|
ENST00000457836.6:c.1293C>T
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ENSP00000416000.2:p.Ala431=
|
|
ENST00000540732.3:c.1386C>T
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ENSP00000443246.1:p.Ala462=
|
|
ENST00000544905.1:c.114C>T
|
|
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ENST00000595085.5:c.922+1857C>T
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ENSP00000471150.2:n.922+1857C>T
|
|
NM_000709.3:c.1284C>T
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NP_000700.1:p.Ala428=
|
|
NM_001164783.1:c.1281C>T
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NP_001158255.1:p.Ala427=
|
|
NM_000709.4:c.1284C>T
MANE Select
|
NP_000700.1:p.Ala428=
|
|
NM_001164783.2:c.1281C>T
|
NP_001158255.1:p.Ala427=
|
|