ENST00000394975.3:c.377T>G
MANE Select
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ENSP00000378426.2:p.Phe126Cys
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ENST00000300851.10:c.438T>G
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ENSP00000300851.6:p.Leu146=
|
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ENST00000319788.11:c.459T>G
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ENSP00000326135.7:p.Leu153=
|
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ENST00000354895.4:c.267T>G
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ENSP00000346969.4:p.Leu89=
|
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ENST00000394971.7:c.471T>G
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ENSP00000378422.3:p.Leu157=
|
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ENST00000394975.2:c.377T>G
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ENSP00000378426.2:p.Phe126Cys
|
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ENST00000420057.2:c.339T>G
|
|
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ENST00000472468.1:c.62T>G
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ENSP00000458994.1:p.Phe21Cys
|
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ENST00000498155.1:c.474T>G
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ENSP00000417662.1:p.Leu158=
|
|
ENST00000529564.1:c.283+2063T>G
|
ENSP00000431371.1:n.283+2063T>G
|
|
ENST00000532364.1:c.173+3308T>G
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ENSP00000460316.1:n.173+3308T>G
|
|
ENST00000533518.5:c.250T>G
|
|
|
NM_001311311.1:c.461T>G
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NP_001298240.1:p.Phe154Cys
|
|
NM_024006.4:c.377T>G
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NP_076869.1:p.Phe126Cys
|
|
NM_024006.5:c.377T>G
|
NP_076869.1:p.Phe126Cys
|
|
NM_206824.1:c.267T>G
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NP_996560.1:p.Leu89=
|
|
NM_206824.2:c.267T>G
|
NP_996560.1:p.Leu89=
|
|
XM_011545944.1:c.377T>G
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XP_011544246.1:p.Phe126Cys
|
|
XM_011545945.1:c.267T>G
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XP_011544247.1:p.Leu89=
|
|
XR_950848.1:n.1165T>G
|
|
|
NM_024006.6:c.377T>G
MANE Select
|
NP_076869.1:p.Phe126Cys
|
|
NM_001311311.2:c.461T>G
|
NP_001298240.1:p.Phe154Cys
|
|
NM_206824.3:c.267T>G
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NP_996560.1:p.Leu89=
|
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