ENST00000394975.3:c.373T>G
MANE Select
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ENSP00000378426.2:p.Phe125Val
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ENST00000300851.10:c.434T>G
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ENSP00000300851.6:p.Val145Gly
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ENST00000319788.11:c.455T>G
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ENSP00000326135.7:p.Val152Gly
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ENST00000354895.4:c.263T>G
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ENSP00000346969.4:p.Val88Gly
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ENST00000394971.7:c.467T>G
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ENSP00000378422.3:p.Val156Gly
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ENST00000394975.2:c.373T>G
|
ENSP00000378426.2:p.Phe125Val
|
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ENST00000420057.2:c.335T>G
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|
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ENST00000472468.1:c.58T>G
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ENSP00000458994.1:p.Phe20Val
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ENST00000498155.1:c.470T>G
|
ENSP00000417662.1:p.Val157Gly
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ENST00000529564.1:c.283+2059T>G
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ENSP00000431371.1:n.283+2059T>G
|
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ENST00000532364.1:c.173+3304T>G
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ENSP00000460316.1:n.173+3304T>G
|
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ENST00000533518.5:c.246T>G
|
|
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NM_001311311.1:c.457T>G
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NP_001298240.1:p.Phe153Val
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NM_024006.4:c.373T>G
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NP_076869.1:p.Phe125Val
|
|
NM_024006.5:c.373T>G
|
NP_076869.1:p.Phe125Val
|
|
NM_206824.1:c.263T>G
|
NP_996560.1:p.Val88Gly
|
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NM_206824.2:c.263T>G
|
NP_996560.1:p.Val88Gly
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XM_011545944.1:c.373T>G
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XP_011544246.1:p.Phe125Val
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XM_011545945.1:c.263T>G
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XP_011544247.1:p.Val88Gly
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XR_950848.1:n.1161T>G
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NM_024006.6:c.373T>G
MANE Select
|
NP_076869.1:p.Phe125Val
|
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NM_001311311.2:c.457T>G
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NP_001298240.1:p.Phe153Val
|
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NM_206824.3:c.263T>G
|
NP_996560.1:p.Val88Gly
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