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|
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|
|
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MANE Select
|
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|
|
|
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|
ENSP00000358549.5:p.Ser455=
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|
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XP_011534257.1:p.Ser142=
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|
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|
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|
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|
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|
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NM_001350511.1:c.839G=
|
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|
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|
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NR_146740.1:n.1784G=
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NR_146749.1:n.1656G=
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NR_146750.1:n.1780G=
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|
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NR_146752.1:n.1724G=
|
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NR_146753.1:n.1576G=
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NR_146754.1:n.1520G=
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NR_146755.1:n.1784G=
|
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NR_146756.1:n.1439G=
|
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NR_146758.1:n.1439G=
|
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NR_146759.1:n.1439G=
|
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XM_011535949.3:c.1364G=
|
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|
|
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|
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|
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|
|
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XM_017011077.2:c.839G=
|
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|
|
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XM_017011078.2:c.839G=
|
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|
|
|
XM_024446494.1:c.839G=
|
XP_024302262.1:p.Ser280=
|
|
|
NM_020320.5:c.1364G=
MANE Select
|
NP_064716.2:p.Ser455=
|
|
|
NM_001318785.2:c.839G=
|
NP_001305714.1:p.Ser280=
|
|
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|
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|
|
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|
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|
NP_001337436.1:p.Ser280=
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|
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NM_001350508.2:c.839G=
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NP_001337437.1:p.Ser280=
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NM_001350509.2:c.839G=
|
NP_001337438.1:p.Ser280=
|
|
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NM_001350510.2:c.839G=
|
NP_001337439.1:p.Ser280=
|
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NM_001350511.2:c.839G=
|
NP_001337440.1:p.Ser280=
|
|
|
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|
|
|
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|
|
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|
NR_146739.2:n.1471G=
|
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|
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|
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NR_146743.2:n.1611G=
|
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|
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|
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|
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|
NR_146747.2:n.1177G=
|
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|
|
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|
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NR_146749.2:n.1611G=
|
|
|
|
NR_146750.2:n.1735G=
|
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NR_146751.2:n.1615G=
|
|
|
|
NR_146752.2:n.1679G=
|
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NR_146753.2:n.1531G=
|
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|
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NR_146754.2:n.1475G=
|
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NR_146755.2:n.1739G=
|
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|
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NR_146756.2:n.1394G=
|
|
|
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NR_146757.2:n.1665G=
|
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NR_146758.2:n.1394G=
|
|
|
|
NR_146759.2:n.1394G=
|
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|
