ENST00000534624.6:c.1343C>T
MANE Select
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ENSP00000432083.1:p.Ala448Val
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ENST00000227378.7:c.1343C>T
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ENSP00000227378.3:p.Ala448Val
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ENST00000453788.6:c.1343C>T
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ENSP00000404372.2:p.Ala448Val
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ENST00000524552.5:c.116C>T
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ENSP00000435908.1:p.Ala39Val
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ENST00000526110.5:c.1286C>T
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ENSP00000433584.1:p.Ala429Val
|
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ENST00000526686.1:c.-2C>T
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ENSP00000435019.1:n.-2C>T
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ENST00000532091.1:n.1318C>T
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|
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ENST00000532636.5:c.1343C>T
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ENSP00000437125.1:p.Ala448Val
|
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ENST00000533238.5:n.445C>T
|
|
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ENST00000533540.5:c.905C>T
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ENSP00000437189.1:p.Ala302Val
|
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ENST00000534319.5:c.635C>T
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ENSP00000433316.1:p.Ala212Val
|
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ENST00000534624.5:c.1343C>T
|
ENSP00000432083.1:p.Ala448Val
|
|
NM_006597.5:c.1343C>T
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NP_006588.1:p.Ala448Val
|
|
NM_153201.3:c.1343C>T
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NP_694881.1:p.Ala448Val
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XM_011542798.1:c.1343C>T
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XP_011541100.1:p.Ala448Val
|
|
NM_006597.6:c.1343C>T
MANE Select
|
NP_006588.1:p.Ala448Val
|
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NM_153201.4:c.1343C>T
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NP_694881.1:p.Ala448Val
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