ENST00000455537.7:c.1082C>G
MANE Select
|
ENSP00000408979.2:p.Ala361Gly
|
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ENST00000674619.1:c.1082C>G
|
ENSP00000502270.1:p.Ala361Gly
|
|
ENST00000675882.1:n.69C>G
|
|
|
ENST00000676081.1:n.228C>G
|
|
|
ENST00000676457.1:c.977C>G
|
ENSP00000501588.1:p.Ala326Gly
|
|
ENST00000286452.5:c.815C>G
|
ENSP00000286452.5:p.Ala272Gly
|
|
ENST00000455537.6:c.1082C>G
|
ENSP00000408979.2:p.Ala361Gly
|
|
NM_004984.2:c.1082C>G
|
NP_004975.2:p.Ala361Gly
|
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NM_001354705.1:c.815C>G
|
NP_001341634.1:p.Ala272Gly
|
|
NM_004984.3:c.1082C>G
|
NP_004975.2:p.Ala361Gly
|
|
XR_002957324.1:n.1315C>G
|
|
|
NM_004984.4:c.1082C>G
MANE Select
|
NP_004975.2:p.Ala361Gly
|
|
NM_001354705.2:c.815C>G
|
NP_001341634.1:p.Ala272Gly
|
|