ENST00000682114.1:c.439T>G
|
ENSP00000507245.1:p.Cys147Gly
|
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ENST00000682478.1:n.629T>G
|
|
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ENST00000683576.1:n.629T>G
|
|
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ENST00000683627.1:c.439T>G
|
ENSP00000507533.1:p.Cys147Gly
|
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ENST00000684082.1:c.396T>G
|
ENSP00000508266.1:n.396T>G
|
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ENST00000684633.1:n.411T>G
|
|
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ENST00000684678.1:c.435T>G
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ENSP00000507059.1:n.435T>G
|
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ENST00000369842.9:c.439T>G
MANE Select
|
ENSP00000358857.4:p.Cys147Gly
|
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ENST00000369835.3:c.334T>G
|
ENSP00000358850.3:p.Cys112Gly
|
|
ENST00000369842.8:c.439T>G
|
ENSP00000358857.4:p.Cys147Gly
|
|
ENST00000428228.5:c.*344T>G
|
ENSP00000401081.1:n.*344T>G
|
|
ENST00000468294.5:n.399T>G
|
|
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ENST00000471965.1:n.228T>G
|
|
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ENST00000485261.1:n.629T>G
|
|
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ENST00000486738.5:n.797T>G
|
|
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ENST00000492448.1:n.422T>G
|
|
|
NM_000117.2:c.439T>G , LRG_745t1:c.439T>G
|
NP_000108.1:p.Cys147Gly
|
|
XM_024452349.1:c.445T>G
|
XP_024308117.1:p.Cys149Gly
|
|
NM_000117.3:c.439T>G
MANE Select
|
NP_000108.1:p.Cys147Gly
|
|