ENST00000449291.7:c.1284C>A
MANE Select
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ENSP00000401508.2:p.Gly428=
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ENST00000340490.7:c.1284C>A
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ENSP00000341136.3:p.Gly428=
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ENST00000426292.7:c.1284C>A
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ENSP00000390949.3:p.Gly428=
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ENST00000435154.7:c.1284C>A
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ENSP00000405670.3:p.Gly428=
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ENST00000449291.6:c.1284C>A
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ENSP00000401508.2:p.Gly428=
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ENST00000460623.5:c.262C>A
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ENST00000464332.5:n.828C>A
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NM_001286829.1:c.1284C>A
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NP_001273758.1:p.Gly428=
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NM_145201.5:c.1284C>A
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NP_660202.3:p.Gly428=
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XM_011517377.1:c.1284C>A
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XP_011515679.1:p.Gly428=
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NM_001363145.1:c.1203C>A
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NP_001350074.1:p.Gly401=
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NM_001363146.1:c.600C>A
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NP_001350075.1:p.Gly200=
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XM_017013975.2:c.1503C>A
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XP_016869464.1:p.Gly501=
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XM_017013976.2:c.1503C>A
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XP_016869465.1:p.Gly501=
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XM_017013977.2:c.1203C>A
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XP_016869466.1:p.Gly401=
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XM_017013978.2:c.1503C>A
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XP_016869467.1:p.Gly501=
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XM_017013979.2:c.600C>A
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XP_016869468.1:p.Gly200=
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XM_024447332.1:c.921C>A
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XP_024303100.1:p.Gly307=
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XM_024447333.1:c.519C>A
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XP_024303101.1:p.Gly173=
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NM_145201.6:c.1284C>A
MANE Select
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NP_660202.3:p.Gly428=
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NM_001286829.2:c.1284C>A
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NP_001273758.1:p.Gly428=
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