ENST00000261769.10:c.2300T>G
MANE Select
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ENSP00000261769.4:p.Phe767Cys
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ENST00000261769.9:c.2300T>G
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ENSP00000261769.4:p.Phe767Cys
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ENST00000422392.6:c.2117T>G
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ENSP00000414946.2:p.Phe706Cys
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ENST00000562118.1:n.518T>G
|
|
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ENST00000562836.5:n.2371T>G
|
|
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ENST00000566510.5:c.*966T>G
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ENSP00000458139.1:n.*966T>G
|
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ENST00000566612.5:c.*540T>G
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ENSP00000454782.1:n.*540T>G
|
|
ENST00000611625.4:c.2363T>G
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ENSP00000481063.1:p.Phe788Cys
|
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ENST00000612417.4:c.1853+3104T>G
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ENSP00000478360.1:n.1853+3104T>G
|
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ENST00000621016.4:c.1866-4545T>G
|
ENSP00000480664.1:n.1866-4545T>G
|
|
NM_004360.3:c.2300T>G , LRG_301t1:c.2300T>G
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NP_004351.1:p.Phe767Cys
|
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XM_011523488.1:c.1565T>G
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XP_011521790.1:p.Phe522Cys
|
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XM_011523489.1:c.1565T>G
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XP_011521791.1:p.Phe522Cys
|
|
NM_001317184.1:c.2117T>G
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NP_001304113.1:p.Phe706Cys
|
|
NM_001317185.1:c.752T>G
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NP_001304114.1:p.Phe251Cys
|
|
NM_001317186.1:c.335T>G
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NP_001304115.1:p.Phe112Cys
|
|
NM_004360.4:c.2300T>G
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NP_004351.1:p.Phe767Cys
|
|
NM_004360.5:c.2300T>G
MANE Select
|
NP_004351.1:p.Phe767Cys
|
|
NM_001317184.2:c.2117T>G
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NP_001304113.1:p.Phe706Cys
|
|
NM_001317185.2:c.752T>G
|
NP_001304114.1:p.Phe251Cys
|
|
NM_001317186.2:c.335T>G
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NP_001304115.1:p.Phe112Cys
|
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