ENST00000495986.2:n.479A>T
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|
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ENST00000682365.1:n.1670A>T
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|
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ENST00000684251.1:n.179A>T
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|
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ENST00000684503.1:n.500A>T
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|
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ENST00000684692.1:c.335A>T
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ENSP00000506792.1:p.Glu112Val
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ENST00000168216.11:c.335A>T
MANE Select
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ENSP00000168216.6:p.Glu112Val
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ENST00000168216.10:c.335A>T
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ENSP00000168216.6:p.Glu112Val
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ENST00000375298.4:c.335A>T
|
ENSP00000364447.4:p.Glu112Val
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|
ENST00000375304.9:c.335A>T
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ENSP00000364453.5:p.Glu112Val
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ENST00000477706.1:n.54A>T
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|
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ENST00000495986.1:n.467A>T
|
|
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NM_001037811.2:c.335A>T , LRG_450t2:c.335A>T
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NP_001032900.1:p.Glu112Val
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NM_004493.2:c.335A>T , LRG_450t1:c.335A>T
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NP_004484.1:p.Glu112Val
|
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NM_004493.3:c.335A>T
MANE Select
|
NP_004484.1:p.Glu112Val
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