ENST00000258385.8:c.1225G>T
MANE Select
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ENSP00000258385.3:p.Gly409Trp
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ENST00000258385.7:c.1225G>T
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ENSP00000258385.3:p.Gly409Trp
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ENST00000441621.6:c.*407G>T
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ENSP00000408819.2:n.*407G>T
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ENST00000446616.1:c.*866G>T
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ENSP00000410801.1:n.*866G>T
|
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ENST00000543200.5:c.1180G>T
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ENSP00000438380.1:p.Gly394Trp
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NM_000751.2:c.1225G>T
|
NP_000742.1:p.Gly409Trp
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NM_001256657.1:c.1180G>T
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NP_001243586.1:p.Gly394Trp
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NM_001311195.1:c.643G>T
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NP_001298124.1:p.Gly215Trp
|
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NM_001311196.1:c.922G>T
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NP_001298125.1:p.Gly308Trp
|
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NR_046333.1:c.-4294966326G>T
|
|
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NR_046334.1:c.-4294966047G>T
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|
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XM_011510524.1:c.844G>T
|
XP_011508826.1:p.Gly282Trp
|
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XM_011510524.2:c.844G>T
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XP_011508826.1:p.Gly282Trp
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NM_000751.3:c.1225G>T
MANE Select
|
NP_000742.1:p.Gly409Trp
|
|
NM_001311195.2:c.643G>T
|
NP_001298124.1:p.Gly215Trp
|
|
NM_001311196.2:c.922G>T
|
NP_001298125.1:p.Gly308Trp
|
|
NM_001256657.2:c.1180G>T
|
NP_001243586.1:p.Gly394Trp
|
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