ENST00000455537.7:c.2955C=
MANE Select
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ENSP00000408979.2:p.Gly985=
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ENST00000674619.1:c.2976C=
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ENSP00000502270.1:p.Gly992=
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|
ENST00000675697.1:c.46C=
|
|
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ENST00000675737.1:n.359C=
|
|
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ENST00000675882.1:n.2478C=
|
|
|
ENST00000675929.1:n.1513C=
|
|
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ENST00000676055.1:c.46C=
|
|
|
ENST00000676457.1:c.2850C=
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ENSP00000501588.1:p.Gly950=
|
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ENST00000286452.5:c.2688C=
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ENSP00000286452.5:p.Gly896=
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ENST00000455537.6:c.2955C=
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ENSP00000408979.2:p.Gly985=
|
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ENST00000552227.1:n.238C=
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|
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NM_004984.2:c.2955C=
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NP_004975.2:p.Gly985=
|
|
NM_001354705.1:c.2688C=
|
NP_001341634.1:p.Gly896=
|
|
NM_004984.3:c.2955C=
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NP_004975.2:p.Gly985=
|
|
XR_002957324.1:n.3188C=
|
|
|
NM_004984.4:c.2955C=
MANE Select
|
NP_004975.2:p.Gly985=
|
|
NM_001354705.2:c.2688C=
|
NP_001341634.1:p.Gly896=
|
|