ENST00000370263.9:c.880G>T
MANE Select
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ENSP00000359285.4:p.Glu294Ter
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ENST00000370263.8:c.880G>T
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ENSP00000359285.4:p.Glu294Ter
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ENST00000463705.5:n.1528G>T
|
|
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ENST00000467563.3:n.950G>T
|
|
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ENST00000498043.6:c.904G>T
|
|
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ENST00000615287.4:c.667G>T
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ENSP00000483388.1:p.Glu223Ter
|
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ENST00000627000.1:c.*569G>T
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ENSP00000486914.1:n.*569G>T
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ENST00000630240.1:n.601G>T
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NM_000744.6:c.880G>T
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NP_000735.1:p.Glu294Ter
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NM_001256573.1:c.352G>T
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NP_001243502.1:p.Glu118Ter
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NR_046317.1:n.1136G>T
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XM_011528524.1:c.667G>T
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XP_011526826.1:p.Glu223Ter
|
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XM_017027625.2:c.352G>T
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XP_016883114.1:p.Glu118Ter
|
|
XM_024451822.1:c.352G>T
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XP_024307590.1:p.Glu118Ter
|
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NM_001256573.2:c.352G>T
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NP_001243502.1:p.Glu118Ter
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NR_046317.2:n.1089G>T
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|
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NM_000744.7:c.880G>T
MANE Select
|
NP_000735.1:p.Glu294Ter
|
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