ENST00000375559.8:c.1421C>T
MANE Select
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ENSP00000364709.3:p.Ala474Val
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ENST00000375551.7:c.*412C>T
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ENSP00000364701.3:n.*412C>T
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|
ENST00000375559.7:c.1421C>T
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ENSP00000364709.3:p.Ala474Val
|
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NM_000504.3:c.1421C>T , LRG_548t1:c.1421C>T
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NP_000495.1:p.Ala474Val
|
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NM_001312674.1:c.1289C>T
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NP_001299603.1:p.Ala430Val
|
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NM_001312675.1:c.*412C>T
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NP_001299604.1:n.*412C>T
|
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NM_000504.4:c.1421C>T
MANE Select
|
NP_000495.1:p.Ala474Val
|
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NM_001312674.2:c.1289C>T
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NP_001299603.1:p.Ala430Val
|
|
NM_001312675.2:c.*412C>T
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NP_001299604.1:n.*412C>T
|
|