ENST00000297598.5:c.1538T=
MANE Select
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ENSP00000297598.4:p.Met513=
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ENST00000297598.4:c.1538T=
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ENSP00000297598.4:p.Met513=
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ENST00000396200.3:c.1613T=
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ENSP00000379503.3:p.Met538=
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ENST00000517764.1:c.1538T=
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ENSP00000430380.1:p.Met513=
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ENST00000520728.5:c.1538T=
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ENSP00000428317.1:p.Met513=
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NM_001161779.1:c.1613T=
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NP_001155251.1:p.Met538=
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NM_001161780.1:c.1613T=
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NP_001155252.1:p.Met538=
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NM_001161781.1:c.1538T=
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NP_001155253.1:p.Met513=
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NM_018444.3:c.1538T=
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NP_060914.2:p.Met513=
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XM_011517135.1:c.1592T=
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XP_011515437.1:p.Met531=
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XM_011517136.1:c.1538T=
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XP_011515438.1:p.Met513=
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XM_011517137.1:c.1538T=
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XP_011515439.1:p.Met513=
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XM_011517135.2:c.1592T=
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XP_011515437.1:p.Met531=
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XM_011517136.2:c.1538T=
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XP_011515438.1:p.Met513=
|
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XM_017013588.1:c.1700T=
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XP_016869077.1:p.Met567=
|
|
NM_018444.4:c.1538T=
MANE Select
|
NP_060914.2:p.Met513=
|
|
NM_001161780.2:c.1613T=
|
NP_001155252.1:p.Met538=
|
|
NM_001161781.2:c.1538T=
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NP_001155253.1:p.Met513=
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NM_001161779.2:c.1613T=
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NP_001155251.1:p.Met538=
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