ENST00000355112.8:c.3658G>T
MANE Select
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ENSP00000347232.3:p.Gly1220Ter
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ENST00000560559.2:n.2231G>T
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ENST00000648453.1:c.3658G>T
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ENSP00000497646.1:p.Gly1220Ter
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ENST00000680772.1:c.3658G>T
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ENSP00000506117.1:p.Gly1220Ter
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ENST00000681142.1:c.3658G>T
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ENSP00000506682.1:p.Gly1220Ter
|
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ENST00000355112.7:c.3658G>T
|
ENSP00000347232.3:p.Gly1220Ter
|
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ENST00000558825.5:n.1005G>T
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ENST00000559724.5:c.*2582G>T
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ENSP00000453359.1:n.*2582G>T
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ENST00000560136.5:n.1684G>T
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ENST00000560509.5:c.3359-4871G>T
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ENSP00000454158.1:n.3359-4871G>T
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NM_000057.3:c.3658G>T
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NP_000048.1:p.Gly1220Ter
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NM_001287246.1:c.3658G>T
|
NP_001274175.1:p.Gly1220Ter
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NM_001287247.1:c.3359-4871G>T
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NP_001274176.1:n.3359-4871G>T
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NM_001287248.1:c.2533G>T
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NP_001274177.1:p.Gly845Ter
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XM_006720632.2:c.1696G>T
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XP_006720695.1:p.Gly566Ter
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XM_011521881.1:c.2344G>T
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XP_011520183.1:p.Gly782Ter
|
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XM_011521881.2:c.2344G>T
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XP_011520183.1:p.Gly782Ter
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NM_000057.4:c.3658G>T
MANE Select
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NP_000048.1:p.Gly1220Ter
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NM_001287246.2:c.3658G>T
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NP_001274175.1:p.Gly1220Ter
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|
NM_001287247.2:c.3359-4871G>T
|
NP_001274176.1:n.3359-4871G>T
|
|
NM_001287248.2:c.2533G>T
|
NP_001274177.1:p.Gly845Ter
|
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