ENST00000328300.11:c.4400G>C
MANE Select
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ENSP00000331902.7:p.Gly1467Ala
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ENST00000361603.7:c.4382G>C
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ENSP00000354505.2:p.Gly1461Ala
|
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ENST00000510690.2:n.894G>C
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ENST00000328300.10:c.4400G>C
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ENSP00000331902.6:p.Gly1467Ala
|
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ENST00000361603.6:c.4382G>C
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ENSP00000354505.2:p.Gly1461Ala
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ENST00000515658.1:c.196G>C
|
|
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NM_000495.4:c.4382G>C
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NP_000486.1:p.Gly1461Ala
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NM_033380.2:c.4400G>C
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NP_203699.1:p.Gly1467Ala
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XM_005262070.2:c.4391G>C
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XP_005262127.1:p.Gly1464Ala
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XM_006724616.2:c.4400G>C
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XP_006724679.1:p.Gly1467Ala
|
|
XM_011530849.1:c.4076G>C
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XP_011529151.1:p.Gly1359Ala
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XM_011530851.1:c.1973G>C
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XP_011529153.1:p.Gly658Ala
|
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XM_011530849.2:c.4415G>C
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XP_011529151.2:p.Gly1472Ala
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XM_017029259.2:c.4406G>C
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XP_016884748.1:p.Gly1469Ala
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XM_017029260.1:c.4397G>C
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XP_016884749.1:p.Gly1466Ala
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XM_017029263.2:c.2735G>C
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XP_016884752.1:p.Gly912Ala
|
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NM_000495.5:c.4382G>C
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NP_000486.1:p.Gly1461Ala
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NM_033380.3:c.4400G>C
MANE Select
|
NP_203699.1:p.Gly1467Ala
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