ENST00000258385.8:c.1369G>T
MANE Select
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ENSP00000258385.3:p.Glu457Ter
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ENST00000258385.7:c.1369G>T
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ENSP00000258385.3:p.Glu457Ter
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ENST00000441621.6:c.*551G>T
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ENSP00000408819.2:n.*551G>T
|
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ENST00000446616.1:c.*1010G>T
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ENSP00000410801.1:n.*1010G>T
|
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ENST00000543200.5:c.1324G>T
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ENSP00000438380.1:p.Glu442Ter
|
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NM_000751.2:c.1369G>T
|
NP_000742.1:p.Glu457Ter
|
|
NM_001256657.1:c.1324G>T
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NP_001243586.1:p.Glu442Ter
|
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NM_001311195.1:c.787G>T
|
NP_001298124.1:p.Glu263Ter
|
|
NM_001311196.1:c.1066G>T
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NP_001298125.1:p.Glu356Ter
|
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NR_046333.1:c.-4294966182G>T
|
|
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NR_046334.1:c.-4294965903G>T
|
|
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XM_011510524.1:c.988G>T
|
XP_011508826.1:p.Glu330Ter
|
|
XM_011510524.2:c.988G>T
|
XP_011508826.1:p.Glu330Ter
|
|
NM_000751.3:c.1369G>T
MANE Select
|
NP_000742.1:p.Glu457Ter
|
|
NM_001311195.2:c.787G>T
|
NP_001298124.1:p.Glu263Ter
|
|
NM_001311196.2:c.1066G>T
|
NP_001298125.1:p.Glu356Ter
|
|
NM_001256657.2:c.1324G>T
|
NP_001243586.1:p.Glu442Ter
|
|