ENST00000256906.5:c.880G>T
MANE Select
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ENSP00000256906.4:p.Glu294Ter
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ENST00000256906.4:c.880G>T
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ENSP00000256906.4:p.Glu294Ter
|
|
ENST00000426880.2:c.616G>T
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ENSP00000402526.2:p.Glu206Ter
|
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NM_001143828.1:c.616G>T
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NP_001137300.1:p.Glu206Ter
|
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NM_001160166.1:c.*512G>T
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NP_001153638.1:n.*512G>T
|
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NM_021624.3:c.880G>T
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NP_067637.2:p.Glu294Ter
|
|
XM_011526133.1:c.357+8318G>T
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XP_011524435.1:n.357+8318G>T
|
|
NM_021624.4:c.880G>T
MANE Select
|
NP_067637.2:p.Glu294Ter
|
|
NM_001143828.2:c.616G>T
|
NP_001137300.1:p.Glu206Ter
|
|
NM_001160166.2:c.*512G>T
|
NP_001153638.1:n.*512G>T
|
|