ENST00000262493.12:c.954A>G
MANE Select
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ENSP00000262493.6:p.Glu318=
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ENST00000562316.6:c.545-1161A>G
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ENSP00000457238.2:n.545-1161A>G
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ENST00000564727.2:c.258A>G
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ENSP00000454971.2:p.Glu86=
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ENST00000568375.2:c.192A>G
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|
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ENST00000638210.1:n.1254A>G
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ENST00000638705.1:c.954A>G
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ENSP00000491223.1:p.Glu318=
|
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ENST00000638836.1:n.864A>G
|
|
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ENST00000639251.1:n.855A>G
|
|
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ENST00000639268.1:c.589A>G
|
|
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ENST00000639341.1:c.479A>G
|
|
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ENST00000639770.1:c.992A>G
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ENSP00000491999.1:n.992A>G
|
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ENST00000640390.1:n.884A>G
|
|
|
ENST00000640469.1:c.318A>G
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ENSP00000491875.1:p.Glu106=
|
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ENST00000640560.1:n.730A>G
|
|
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ENST00000640893.1:c.*352A>G
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ENSP00000492677.1:n.*352A>G
|
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ENST00000262493.10:c.954A>G
|
ENSP00000262493.6:p.Glu318=
|
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ENST00000564727.1:c.174A>G
|
ENSP00000454971.1:p.Glu58=
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ENST00000568375.1:n.192A>G
|
|
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NM_020988.2:c.954A>G
|
NP_066268.1:p.Glu318=
|
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XM_011523003.1:c.828A>G
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XP_011521305.1:p.Glu276=
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XM_011523003.3:c.828A>G
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XP_011521305.1:p.Glu276=
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NM_020988.3:c.954A>G
MANE Select
|
NP_066268.1:p.Glu318=
|
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