ENST00000553106.6:c.1065G>A
MANE Select
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ENSP00000448059.1:p.Gln355=
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ENST00000307000.7:c.1050G>A
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ENSP00000303500.2:p.Gln350=
|
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ENST00000549247.6:n.824G>A
|
|
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ENST00000551114.2:n.727G>A
|
|
|
ENST00000553106.5:c.1065G>A
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ENSP00000448059.1:p.Gln355=
|
|
ENST00000635477.1:c.169G>A
|
|
|
ENST00000635528.1:n.580G>A
|
|
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NM_000277.1:c.1065G>A
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NP_000268.1:p.Gln355=
|
|
XM_011538422.1:c.1008G>A
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XP_011536724.1:p.Gln336=
|
|
NM_000277.2:c.1065G>A
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NP_000268.1:p.Gln355=
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NM_001354304.1:c.1065G>A
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NP_001341233.1:p.Gln355=
|
|
NM_000277.3:c.1065G>A
MANE Select
|
NP_000268.1:p.Gln355=
|
|
NM_001354304.2:c.1065G>A
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NP_001341233.1:p.Gln355=
|
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