ENST00000553591.2:c.612C>T
|
ENSP00000452421.2:p.Ala204=
|
|
ENST00000556293.6:n.2918C>T
|
|
|
ENST00000556754.2:n.3861C>T
|
|
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ENST00000557229.6:n.924C>T
|
|
|
ENST00000697613.1:c.495C>T
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ENSP00000513359.1:p.Ala165=
|
|
ENST00000697614.1:c.258C>T
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ENSP00000513360.1:p.Ala86=
|
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ENST00000697615.1:n.1323C>T
|
|
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ENST00000361505.10:c.495C>T
MANE Select
|
ENSP00000354532.6:p.Ala165=
|
|
ENST00000361505.9:c.495C>T
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ENSP00000354532.5:p.Ala165=
|
|
ENST00000553591.1:c.612C>T
|
ENSP00000452421.1:p.Ala204=
|
|
ENST00000554056.5:n.803C>T
|
|
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ENST00000556754.1:n.1712C>T
|
|
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ENST00000557229.5:n.924C>T
|
|
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NM_000270.3:c.495C>T , LRG_91t1:c.495C>T
|
NP_000261.2:p.Ala165=
|
|
NM_000270.4:c.495C>T
MANE Select
|
NP_000261.2:p.Ala165=
|
|