ENST00000222248.4:c.1699C=
MANE Select
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ENSP00000222248.2:p.Leu567=
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ENST00000222248.3:c.1699C=
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ENSP00000222248.2:p.Leu567=
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NM_000453.2:c.1699C=
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NP_000444.1:p.Leu567=
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XM_011528192.1:c.1732C=
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XP_011526494.1:p.Leu578=
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XM_011528193.1:c.1465C=
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XP_011526495.1:p.Leu489=
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XM_011528194.1:c.1366C=
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XP_011526496.1:p.Leu456=
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|
XM_011528192.2:c.1732C=
|
XP_011526494.1:p.Leu578=
|
|
XM_011528193.3:c.1465C=
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XP_011526495.1:p.Leu489=
|
|
XM_011528194.3:c.1366C=
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XP_011526496.1:p.Leu456=
|
|
XM_017027158.1:c.1432C=
|
XP_016882647.1:p.Leu478=
|
|
NM_000453.3:c.1699C=
MANE Select
|
NP_000444.1:p.Leu567=
|
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