ENST00000449291.7:c.1577A>T
MANE Select
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ENSP00000401508.2:p.Gln526Leu
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ENST00000340490.7:c.1662A>T
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ENSP00000341136.3:p.Ala554=
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ENST00000426292.7:c.1538A>T
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ENSP00000390949.3:p.Gln513Leu
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ENST00000435154.7:c.*286A>T
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ENSP00000405670.3:n.*286A>T
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ENST00000449291.6:c.1577A>T
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ENSP00000401508.2:p.Gln526Leu
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ENST00000460623.5:c.601A>T
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|
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ENST00000464332.5:n.1121A>T
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|
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ENST00000498076.5:n.356A>T
|
|
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ENST00000529179.1:n.361A>T
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NM_001286829.1:c.1538A>T
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NP_001273758.1:p.Gln513Leu
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NM_145201.5:c.1577A>T
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NP_660202.3:p.Gln526Leu
|
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XM_011517377.1:c.1314A>T
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XP_011515679.1:p.Ala438=
|
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NM_001363145.1:c.1496A>T
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NP_001350074.1:p.Gln499Leu
|
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NM_001363146.1:c.893A>T
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NP_001350075.1:p.Gln298Leu
|
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XM_017013975.2:c.1881A>T
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XP_016869464.1:p.Ala627=
|
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XM_017013976.2:c.1796A>T
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XP_016869465.1:p.Gln599Leu
|
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XM_017013977.2:c.1581A>T
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XP_016869466.1:p.Ala527=
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XM_017013978.2:c.1533A>T
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XP_016869467.1:p.Ala511=
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XM_017013979.2:c.978A>T
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XP_016869468.1:p.Ala326=
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XM_024447332.1:c.951A>T
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XP_024303100.1:p.Ala317=
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XM_024447333.1:c.897A>T
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XP_024303101.1:p.Ala299=
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NM_145201.6:c.1577A>T
MANE Select
|
NP_660202.3:p.Gln526Leu
|
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NM_001286829.2:c.1538A>T
|
NP_001273758.1:p.Gln513Leu
|
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