ENST00000248633.9:c.1806A>T
MANE Select
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ENSP00000248633.4:p.Gly602=
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ENST00000248633.8:c.1806A>T
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ENSP00000248633.4:p.Gly602=
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ENST00000422866.1:c.624A>T
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ENST00000428214.5:c.1806A>T
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ENSP00000394413.1:p.Gly602=
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ENST00000438045.5:c.840A>T
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ENSP00000410438.1:p.Gly280=
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ENST00000484913.5:n.1845A>T
|
|
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ENST00000496420.5:n.1482A>T
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NM_000466.2:c.1806A>T
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NP_000457.1:p.Gly602=
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NM_001282677.1:c.1806A>T
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NP_001269606.1:p.Gly602=
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NM_001282678.1:c.1182A>T
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NP_001269607.1:p.Gly394=
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XM_005250433.3:c.57A>T
|
XP_005250490.1:p.Gly19=
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XR_242246.3:n.1902A>T
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XM_017012319.2:c.57A>T
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XP_016867808.1:p.Gly19=
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XR_001744808.2:n.833A>T
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XR_242246.5:n.1853A>T
|
|
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NM_000466.3:c.1806A>T
MANE Select
|
NP_000457.1:p.Gly602=
|
|
NM_001282677.2:c.1806A>T
|
NP_001269606.1:p.Gly602=
|
|
NM_001282678.2:c.1182A>T
|
NP_001269607.1:p.Gly394=
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