ENST00000269980.7:c.1253C>G
MANE Select
|
ENSP00000269980.2:p.Ala418Gly
|
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ENST00000269980.6:c.1253C>G
|
ENSP00000269980.2:p.Ala418Gly
|
|
ENST00000457836.6:c.1262C>G
|
ENSP00000416000.2:p.Ala421Gly
|
|
ENST00000540732.3:c.1355C>G
|
ENSP00000443246.1:p.Ala452Gly
|
|
ENST00000544905.1:c.83C>G
|
|
|
ENST00000595085.5:c.922+1826C>G
|
ENSP00000471150.2:n.922+1826C>G
|
|
NM_000709.3:c.1253C>G
|
NP_000700.1:p.Ala418Gly
|
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NM_001164783.1:c.1250C>G
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NP_001158255.1:p.Ala417Gly
|
|
NM_000709.4:c.1253C>G
MANE Select
|
NP_000700.1:p.Ala418Gly
|
|
NM_001164783.2:c.1250C>G
|
NP_001158255.1:p.Ala417Gly
|
|