ENST00000053867.8:c.1163G>T
MANE Select
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ENSP00000053867.2:p.Cys388Phe
|
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ENST00000639447.1:c.1136+27G>T
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ENSP00000492014.1:n.1136+27G>T
|
|
ENST00000053867.7:c.1163G>T
|
ENSP00000053867.2:p.Cys388Phe
|
|
ENST00000586443.1:c.604G>T
|
|
|
ENST00000589265.5:c.692G>T
|
ENSP00000467616.1:p.Cys231Phe
|
|
ENST00000589923.1:n.421G>T
|
|
|
NM_002087.3:c.1163G>T
|
NP_002078.1:p.Cys388Phe
|
|
XM_005257253.1:c.1163G>T
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XP_005257310.1:p.Cys388Phe
|
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XM_024450730.1:c.1163G>T
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XP_024306498.1:p.Cys388Phe
|
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NM_002087.4:c.1163G>T
MANE Select
|
NP_002078.1:p.Cys388Phe
|
|