ENST00000292408.9:c.1166T=
MANE Select
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ENSP00000292408.4:p.Leu389=
|
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ENST00000292408.8:c.1166T=
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ENSP00000292408.4:p.Leu389=
|
|
ENST00000393637.5:c.1058-86T=
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ENSP00000377254.1:n.1058-86T=
|
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ENST00000393648.6:c.1097+69T=
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ENSP00000377259.2:n.1097+69T=
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|
ENST00000502906.5:c.1166T=
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ENSP00000424960.1:p.Leu389=
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|
ENST00000508139.1:n.470T=
|
|
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ENST00000511076.1:c.72T=
|
|
|
NM_001291980.1:c.1097+69T=
|
NP_001278909.1:n.1097+69T=
|
|
NM_002011.4:c.1166T=
|
NP_002002.3:p.Leu389=
|
|
NM_022963.3:c.1058-86T=
|
NP_075252.2:n.1058-86T=
|
|
NM_213647.2:c.1166T=
|
NP_998812.1:p.Leu389=
|
|
XM_005265838.2:c.1166T=
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XP_005265895.1:p.Leu389=
|
|
XM_011534464.1:c.1259T=
|
XP_011532766.1:p.Leu420=
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|
XM_011534465.1:c.848T=
|
XP_011532767.1:p.Leu283=
|
|
XR_941090.1:n.1211T=
|
|
|
NM_001354984.1:c.1166T=
|
NP_001341913.1:p.Leu389=
|
|
NM_213647.3:c.1166T=
MANE Select
|
NP_998812.1:p.Leu389=
|
|
NM_001291980.2:c.1097+69T=
|
NP_001278909.1:n.1097+69T=
|
|
NM_001354984.2:c.1166T=
|
NP_001341913.1:p.Leu389=
|
|
NM_002011.5:c.1166T=
|
NP_002002.3:p.Leu389=
|
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