ENST00000053867.8:c.1160G>T
MANE Select
|
ENSP00000053867.2:p.Gly387Val
|
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ENST00000639447.1:c.1136+24G>T
|
ENSP00000492014.1:n.1136+24G>T
|
|
ENST00000053867.7:c.1160G>T
|
ENSP00000053867.2:p.Gly387Val
|
|
ENST00000586443.1:c.601G>T
|
|
|
ENST00000589265.5:c.689G>T
|
ENSP00000467616.1:p.Gly230Val
|
|
ENST00000589923.1:n.418G>T
|
|
|
NM_002087.3:c.1160G>T
|
NP_002078.1:p.Gly387Val
|
|
XM_005257253.1:c.1160G>T
|
XP_005257310.1:p.Gly387Val
|
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XM_024450730.1:c.1160G>T
|
XP_024306498.1:p.Gly387Val
|
|
NM_002087.4:c.1160G>T
MANE Select
|
NP_002078.1:p.Gly387Val
|
|