ENST00000334554.12:c.408G>T
MANE Select
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ENSP00000334490.7:p.Trp136Cys
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ENST00000320602.11:c.384+108G>T
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ENSP00000317804.7:n.384+108G>T
|
|
ENST00000334554.11:c.408G>T
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ENSP00000334490.7:p.Trp136Cys
|
|
ENST00000405930.3:c.408G>T
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ENSP00000384716.3:p.Trp136Cys
|
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ENST00000436518.5:c.375G>T
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ENSP00000412807.1:p.Trp125Cys
|
|
ENST00000468112.5:n.58-874G>T
|
|
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NM_001185024.1:c.408G>T
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NP_001171953.1:p.Trp136Cys
|
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NM_013373.3:c.408G>T
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NP_037505.1:p.Trp136Cys
|
|
XM_006724239.2:c.408G>T
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XP_006724302.1:p.Trp136Cys
|
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NM_001185024.2:c.408G>T
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NP_001171953.1:p.Trp136Cys
|
|
NM_013373.4:c.408G>T
MANE Select
|
NP_037505.1:p.Trp136Cys
|
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