ENST00000356392.9:c.1307A>T
MANE Select
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ENSP00000348757.3:p.Glu436Val
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|
ENST00000356392.8:c.1307A>T
|
ENSP00000348757.3:p.Glu436Val
|
|
ENST00000586836.5:c.734A>T
|
ENSP00000467429.1:p.Glu245Val
|
|
ENST00000591179.5:c.1127A>T
|
ENSP00000466800.1:p.Glu376Val
|
|
ENST00000591345.5:c.*1226A>T
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ENSP00000467313.1:n.*1226A>T
|
|
NM_001302453.1:c.1145A>T
|
NP_001289382.1:p.Glu382Val
|
|
NM_001302454.1:c.1127A>T
|
NP_001289383.1:p.Glu376Val
|
|
NM_145045.4:c.1307A>T
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NP_659482.3:p.Glu436Val
|
|
NM_145045.5:c.1307A>T
MANE Select
|
NP_659482.3:p.Glu436Val
|
|
NM_001302454.2:c.1127A>T
|
NP_001289383.1:p.Glu376Val
|
|