ENST00000322776.11:c.586T>G
MANE Select
|
ENSP00000322450.6:p.Phe196Val
|
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ENST00000647561.1:c.586T>G
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ENSP00000497587.1:p.Phe196Val
|
|
ENST00000322776.10:c.586T>G
|
ENSP00000322450.6:p.Phe196Val
|
|
ENST00000415352.6:c.565T>G
|
ENSP00000395368.2:p.Phe189Val
|
|
ENST00000526169.1:n.328T>G
|
|
|
ENST00000526770.5:n.445T>G
|
|
|
ENST00000529927.5:c.559T>G
|
ENSP00000436766.1:p.Phe187Val
|
|
ENST00000532244.5:c.283T>G
|
ENSP00000435202.1:p.Phe95Val
|
|
ENST00000532303.5:c.283T>G
|
ENSP00000432015.1:p.Phe95Val
|
|
ENST00000532343.5:c.283T>G
|
ENSP00000431751.1:p.Phe95Val
|
|
ENST00000533919.5:c.64T>G
|
ENSP00000435199.1:p.Phe22Val
|
|
NM_001166102.1:c.559T>G
|
NP_001159574.1:p.Phe187Val
|
|
NM_007103.3:c.586T>G
|
NP_009034.2:p.Phe196Val
|
|
NM_001166102.2:c.559T>G
|
NP_001159574.1:p.Phe187Val
|
|
NM_007103.4:c.586T>G
MANE Select
|
NP_009034.2:p.Phe196Val
|
|