ENST00000334256.9:c.1215T=
MANE Select
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ENSP00000334373.4:p.Ala405=
|
|
ENST00000483437.2:c.1215T=
|
ENSP00000417172.2:p.Ala405=
|
|
ENST00000676799.1:c.*1164T=
|
ENSP00000503839.1:n.*1164T=
|
|
ENST00000676866.1:c.1143T=
|
ENSP00000503291.1:p.Ala381=
|
|
ENST00000676958.1:c.1327T=
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ENSP00000503083.1:n.1327T=
|
|
ENST00000678020.1:n.1395T=
|
|
|
ENST00000678630.1:c.*1180T=
|
ENSP00000504510.1:n.*1180T=
|
|
ENST00000678765.1:c.1083T=
|
ENSP00000503064.1:p.Ala361=
|
|
ENST00000334256.8:c.1215T=
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ENSP00000334373.4:p.Ala405=
|
|
ENST00000483437.1:c.258T=
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ENSP00000417172.1:p.Ala86=
|
|
NM_002268.4:c.1215T=
|
NP_002259.1:p.Ala405=
|
|
NM_002268.5:c.1215T=
MANE Select
|
NP_002259.1:p.Ala405=
|
|