ENST00000553106.6:c.1189G>T
MANE Select
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ENSP00000448059.1:p.Glu397Ter
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ENST00000307000.7:c.1174G>T
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ENSP00000303500.2:p.Glu392Ter
|
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ENST00000549247.6:n.948G>T
|
|
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ENST00000551114.2:n.851G>T
|
|
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ENST00000553106.5:c.1189G>T
|
ENSP00000448059.1:p.Glu397Ter
|
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ENST00000635477.1:c.293G>T
|
|
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ENST00000635528.1:n.704G>T
|
|
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NM_000277.1:c.1189G>T
|
NP_000268.1:p.Glu397Ter
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XM_011538422.1:c.1132G>T
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XP_011536724.1:p.Glu378Ter
|
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NM_000277.2:c.1189G>T
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NP_000268.1:p.Glu397Ter
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NM_001354304.1:c.1189G>T
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NP_001341233.1:p.Glu397Ter
|
|
NM_000277.3:c.1189G>T
MANE Select
|
NP_000268.1:p.Glu397Ter
|
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NM_001354304.2:c.1189G>T
|
NP_001341233.1:p.Glu397Ter
|
|