ENST00000356392.9:c.1308G>A
MANE Select
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ENSP00000348757.3:p.Glu436=
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ENST00000356392.8:c.1308G>A
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ENSP00000348757.3:p.Glu436=
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|
ENST00000586836.5:c.735G>A
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ENSP00000467429.1:p.Glu245=
|
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ENST00000591179.5:c.1128G>A
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ENSP00000466800.1:p.Glu376=
|
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ENST00000591345.5:c.*1227G>A
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ENSP00000467313.1:n.*1227G>A
|
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NM_001302453.1:c.1146G>A
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NP_001289382.1:p.Glu382=
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NM_001302454.1:c.1128G>A
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NP_001289383.1:p.Glu376=
|
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NM_145045.4:c.1308G>A
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NP_659482.3:p.Glu436=
|
|
NM_145045.5:c.1308G>A
MANE Select
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NP_659482.3:p.Glu436=
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NM_001302454.2:c.1128G>A
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NP_001289383.1:p.Glu376=
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