ENST00000449291.7:c.1593T=
MANE Select
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ENSP00000401508.2:p.Ser531=
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ENST00000340490.7:c.1678T=
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ENSP00000341136.3:p.Ser560=
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ENST00000426292.7:c.1554T=
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ENSP00000390949.3:p.Ser518=
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ENST00000435154.7:c.*302T=
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ENSP00000405670.3:n.*302T=
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ENST00000449291.6:c.1593T=
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ENSP00000401508.2:p.Ser531=
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ENST00000460623.5:c.617T=
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ENST00000464332.5:n.1137T=
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ENST00000498076.5:n.372T=
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ENST00000529179.1:n.377T=
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NM_001286829.1:c.1554T=
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NP_001273758.1:p.Ser518=
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NM_145201.5:c.1593T=
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NP_660202.3:p.Ser531=
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XM_011517377.1:c.1330T=
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XP_011515679.1:p.Ser444=
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NM_001363145.1:c.1512T=
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NP_001350074.1:p.Ser504=
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NM_001363146.1:c.909T=
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NP_001350075.1:p.Ser303=
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XM_017013975.2:c.1897T=
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XP_016869464.1:p.Ser633=
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XM_017013976.2:c.1812T=
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XP_016869465.1:p.Ser604=
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XM_017013977.2:c.1597T=
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XP_016869466.1:p.Ser533=
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XM_017013978.2:c.1549T=
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XP_016869467.1:p.Ser517=
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XM_017013979.2:c.994T=
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XP_016869468.1:p.Ser332=
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XM_024447332.1:c.967T=
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XP_024303100.1:p.Ser323=
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XM_024447333.1:c.913T=
|
XP_024303101.1:p.Ser305=
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NM_145201.6:c.1593T=
MANE Select
|
NP_660202.3:p.Ser531=
|
|
NM_001286829.2:c.1554T=
|
NP_001273758.1:p.Ser518=
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