ENST00000356392.9:c.1296C>G
MANE Select
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ENSP00000348757.3:p.Ala432=
|
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ENST00000356392.8:c.1296C>G
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ENSP00000348757.3:p.Ala432=
|
|
ENST00000586836.5:c.723C>G
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ENSP00000467429.1:p.Ala241=
|
|
ENST00000591179.5:c.1116C>G
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ENSP00000466800.1:p.Ala372=
|
|
ENST00000591345.5:c.*1215C>G
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ENSP00000467313.1:n.*1215C>G
|
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NM_001302453.1:c.1134C>G
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NP_001289382.1:p.Ala378=
|
|
NM_001302454.1:c.1116C>G
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NP_001289383.1:p.Ala372=
|
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NM_145045.4:c.1296C>G
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NP_659482.3:p.Ala432=
|
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NM_145045.5:c.1296C>G
MANE Select
|
NP_659482.3:p.Ala432=
|
|
NM_001302454.2:c.1116C>G
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NP_001289383.1:p.Ala372=
|
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