ENST00000336906.6:c.127T>G
MANE Select
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ENSP00000338082.4:p.Phe43Val
|
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ENST00000380252.6:c.-39T>G
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ENSP00000369602.2:n.-39T>G
|
|
ENST00000380259.7:c.1673T>G
|
ENSP00000369609.3:n.1673T>G
|
|
ENST00000642908.1:c.127T>G
|
ENSP00000495346.1:p.Phe43Val
|
|
ENST00000647543.1:c.127T>G
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ENSP00000496470.1:p.Phe43Val
|
|
ENST00000336906.4:c.127T>G
|
ENSP00000338082.4:p.Phe43Val
|
|
ENST00000380252.5:c.97T>G
|
ENSP00000369602.1:p.Phe33Val
|
|
ENST00000380259.6:c.127T>G
|
ENSP00000369609.2:p.Phe43Val
|
|
ENST00000444587.1:c.89T>G
|
ENSP00000488218.1:p.Leu30Arg
|
|
ENST00000620888.4:c.127T>G
|
ENSP00000479637.1:p.Phe43Val
|
|
ENST00000624109.1:c.228A>C
|
ENSP00000485458.1:p.Lys76Asn
|
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NM_000184.2:c.127T>G
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NP_000175.1:p.Phe43Val
|
|
NM_000184.3:c.127T>G
MANE Select
|
NP_000175.1:p.Phe43Val
|
|