ENST00000309755.9:c.1551G>C
MANE Select
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ENSP00000312397.4:p.Trp517Cys
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|
ENST00000309755.8:c.1551G>C
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ENSP00000312397.4:p.Trp517Cys
|
|
ENST00000447439.6:n.1607G>C
|
|
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ENST00000504208.5:c.*435G>C
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ENSP00000423585.1:n.*435G>C
|
|
ENST00000506491.5:c.1305G>C
|
ENSP00000424828.1:p.Trp435Cys
|
|
ENST00000506873.5:n.1074G>C
|
|
|
ENST00000508657.5:c.1455G>C
|
ENSP00000422099.1:p.Trp485Cys
|
|
ENST00000509694.1:n.344G>C
|
|
|
NM_001257194.1:c.1455G>C
|
NP_001244123.1:p.Trp485Cys
|
|
NM_001257195.1:c.1305G>C
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NP_001244124.1:p.Trp435Cys
|
|
NM_017415.2:c.1551G>C
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NP_059111.2:p.Trp517Cys
|
|
NM_017415.3:c.1551G>C
MANE Select
|
NP_059111.2:p.Trp517Cys
|
|
NM_001257195.2:c.1305G>C
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NP_001244124.1:p.Trp435Cys
|
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