ENST00000449291.7:c.1383G>A
MANE Select
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ENSP00000401508.2:p.Glu461=
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ENST00000340490.7:c.1383G>A
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ENSP00000341136.3:p.Glu461=
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ENST00000426292.7:c.1383G>A
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ENSP00000390949.3:p.Glu461=
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ENST00000435154.7:c.1383G>A
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ENSP00000405670.3:p.Glu461=
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ENST00000449291.6:c.1383G>A
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ENSP00000401508.2:p.Glu461=
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ENST00000460623.5:c.361G>A
|
|
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ENST00000464332.5:n.927G>A
|
|
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ENST00000498076.5:n.162G>A
|
|
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ENST00000529179.1:n.70G>A
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NM_001286829.1:c.1383G>A
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NP_001273758.1:p.Glu461=
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NM_145201.5:c.1383G>A
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NP_660202.3:p.Glu461=
|
|
XM_011517377.1:c.1291+169G>A
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XP_011515679.1:n.1291+169G>A
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NM_001363145.1:c.1302G>A
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NP_001350074.1:p.Glu434=
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NM_001363146.1:c.699G>A
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NP_001350075.1:p.Glu233=
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XM_017013975.2:c.1602G>A
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XP_016869464.1:p.Glu534=
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|
XM_017013976.2:c.1602G>A
|
XP_016869465.1:p.Glu534=
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XM_017013977.2:c.1302G>A
|
XP_016869466.1:p.Glu434=
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XM_017013978.2:c.1510+169G>A
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XP_016869467.1:n.1510+169G>A
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XM_017013979.2:c.699G>A
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XP_016869468.1:p.Glu233=
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XM_024447332.1:c.928+169G>A
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XP_024303100.1:n.928+169G>A
|
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XM_024447333.1:c.618G>A
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XP_024303101.1:p.Glu206=
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NM_145201.6:c.1383G>A
MANE Select
|
NP_660202.3:p.Glu461=
|
|
NM_001286829.2:c.1383G>A
|
NP_001273758.1:p.Glu461=
|
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