ENST00000274576.9:c.889G=
MANE Select
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ENSP00000274576.5:p.Gly297=
|
|
ENST00000274576.8:c.889G=
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ENSP00000274576.4:p.Gly297=
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|
ENST00000455880.2:c.889G=
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ENSP00000411593.2:p.Gly297=
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|
ENST00000462581.6:c.*647G=
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ENSP00000430595.1:n.*647G=
|
|
ENST00000471351.2:n.1172G=
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|
|
NM_000171.3:c.889G=
|
NP_000162.2:p.Gly297=
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|
NM_001146040.1:c.889G=
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NP_001139512.1:p.Gly297=
|
|
NM_001292000.1:c.640G=
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NP_001278929.1:p.Gly214=
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|
XM_005268412.2:c.889G=
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XP_005268469.1:p.Gly297=
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|
NM_000171.4:c.889G=
MANE Select
|
NP_000162.2:p.Gly297=
|
|
NM_001146040.2:c.889G=
|
NP_001139512.1:p.Gly297=
|
|
NM_001292000.2:c.640G=
|
NP_001278929.1:p.Gly214=
|
|