ENST00000322776.11:c.587T=
MANE Select
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ENSP00000322450.6:p.Phe196=
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ENST00000647561.1:c.587T=
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ENSP00000497587.1:p.Phe196=
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|
ENST00000322776.10:c.587T=
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ENSP00000322450.6:p.Phe196=
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|
ENST00000415352.6:c.566T=
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ENSP00000395368.2:p.Phe189=
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|
ENST00000526169.1:n.329T=
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|
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ENST00000526770.5:n.446T=
|
|
|
ENST00000529927.5:c.560T=
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ENSP00000436766.1:p.Phe187=
|
|
ENST00000532244.5:c.284T=
|
ENSP00000435202.1:p.Phe95=
|
|
ENST00000532303.5:c.284T=
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ENSP00000432015.1:p.Phe95=
|
|
ENST00000532343.5:c.284T=
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ENSP00000431751.1:p.Phe95=
|
|
ENST00000533919.5:c.65T=
|
ENSP00000435199.1:p.Phe22=
|
|
NM_001166102.1:c.560T=
|
NP_001159574.1:p.Phe187=
|
|
NM_007103.3:c.587T=
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NP_009034.2:p.Phe196=
|
|
NM_001166102.2:c.560T=
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NP_001159574.1:p.Phe187=
|
|
NM_007103.4:c.587T=
MANE Select
|
NP_009034.2:p.Phe196=
|
|