ENST00000450114.7:c.1436A>C
MANE Select
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ENSP00000402084.2:p.Asp479Ala
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ENST00000530712.6:c.254A>C
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ENSP00000434148.2:p.Asp85Ala
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ENST00000680141.1:c.*386A>C
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ENSP00000506686.1:n.*386A>C
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ENST00000681684.1:c.794A>C
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ENSP00000506667.1:p.Asp265Ala
|
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ENST00000299613.10:c.794A>C
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ENSP00000299613.5:p.Asp265Ala
|
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ENST00000450114.6:c.1436A>C
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ENSP00000402084.2:p.Asp479Ala
|
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ENST00000524612.5:c.320A>C
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ENSP00000434446.1:p.Asp107Ala
|
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ENST00000530175.5:c.283A>C
|
|
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ENST00000530712.5:c.254A>C
|
ENSP00000434148.1:p.Asp85Ala
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ENST00000532275.1:n.223A>C
|
|
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NM_001143976.1:c.794A>C
|
NP_001137448.1:p.Asp265Ala
|
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NM_003390.3:c.1436A>C
|
NP_003381.1:p.Asp479Ala
|
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XM_005253118.3:c.1436A>C
|
XP_005253175.1:p.Asp479Ala
|
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XM_005253119.3:c.794A>C
|
XP_005253176.1:p.Asp265Ala
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NM_003390.4:c.1436A>C
MANE Select
|
NP_003381.1:p.Asp479Ala
|
|
NM_001143976.2:c.794A>C
|
NP_001137448.1:p.Asp265Ala
|
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