ENST00000449291.7:c.1584G>T
MANE Select
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ENSP00000401508.2:p.Leu528=
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ENST00000340490.7:c.1669G>T
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ENSP00000341136.3:p.Gly557Cys
|
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ENST00000426292.7:c.1545G>T
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ENSP00000390949.3:p.Leu515=
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ENST00000435154.7:c.*293G>T
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ENSP00000405670.3:n.*293G>T
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ENST00000449291.6:c.1584G>T
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ENSP00000401508.2:p.Leu528=
|
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ENST00000460623.5:c.608G>T
|
|
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ENST00000464332.5:n.1128G>T
|
|
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ENST00000498076.5:n.363G>T
|
|
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ENST00000529179.1:n.368G>T
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|
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NM_001286829.1:c.1545G>T
|
NP_001273758.1:p.Leu515=
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NM_145201.5:c.1584G>T
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NP_660202.3:p.Leu528=
|
|
XM_011517377.1:c.1321G>T
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XP_011515679.1:p.Gly441Cys
|
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NM_001363145.1:c.1503G>T
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NP_001350074.1:p.Leu501=
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|
NM_001363146.1:c.900G>T
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NP_001350075.1:p.Leu300=
|
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XM_017013975.2:c.1888G>T
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XP_016869464.1:p.Gly630Cys
|
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XM_017013976.2:c.1803G>T
|
XP_016869465.1:p.Leu601=
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XM_017013977.2:c.1588G>T
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XP_016869466.1:p.Gly530Cys
|
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XM_017013978.2:c.1540G>T
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XP_016869467.1:p.Gly514Cys
|
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XM_017013979.2:c.985G>T
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XP_016869468.1:p.Gly329Cys
|
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XM_024447332.1:c.958G>T
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XP_024303100.1:p.Gly320Cys
|
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XM_024447333.1:c.904G>T
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XP_024303101.1:p.Gly302Cys
|
|
NM_145201.6:c.1584G>T
MANE Select
|
NP_660202.3:p.Leu528=
|
|
NM_001286829.2:c.1545G>T
|
NP_001273758.1:p.Leu515=
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