ENST00000274576.9:c.1079G>C
MANE Select
|
ENSP00000274576.5:p.Gly360Ala
|
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ENST00000274576.8:c.1079G>C
|
ENSP00000274576.4:p.Gly360Ala
|
|
ENST00000455880.2:c.1103G>C
|
ENSP00000411593.2:p.Gly368Ala
|
|
ENST00000462581.6:c.*837G>C
|
ENSP00000430595.1:n.*837G>C
|
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NM_000171.3:c.1079G>C
|
NP_000162.2:p.Gly360Ala
|
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NM_001146040.1:c.1103G>C
|
NP_001139512.1:p.Gly368Ala
|
|
NM_001292000.1:c.830G>C
|
NP_001278929.1:p.Gly277Ala
|
|
NM_000171.4:c.1079G>C
MANE Select
|
NP_000162.2:p.Gly360Ala
|
|
NM_001146040.2:c.1103G>C
|
NP_001139512.1:p.Gly368Ala
|
|
NM_001292000.2:c.830G>C
|
NP_001278929.1:p.Gly277Ala
|
|