ENST00000328300.11:c.3880G>T
MANE Select
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ENSP00000331902.7:p.Gly1294Cys
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ENST00000361603.7:c.3862G>T
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ENSP00000354505.2:p.Gly1288Cys
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ENST00000510690.2:n.374G>T
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ENST00000328300.10:c.3880G>T
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ENSP00000331902.6:p.Gly1294Cys
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ENST00000361603.6:c.3862G>T
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ENSP00000354505.2:p.Gly1288Cys
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ENST00000489230.1:n.283G>T
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ENST00000510690.1:n.374G>T
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NM_000495.4:c.3862G>T
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NP_000486.1:p.Gly1288Cys
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NM_033380.2:c.3880G>T
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NP_203699.1:p.Gly1294Cys
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XM_005262070.2:c.3871G>T
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XP_005262127.1:p.Gly1291Cys
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XM_006724616.2:c.3880G>T
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XP_006724679.1:p.Gly1294Cys
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XM_011530849.1:c.3556G>T
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XP_011529151.1:p.Gly1186Cys
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XM_011530851.1:c.1453G>T
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XP_011529153.1:p.Gly485Cys
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XM_011530849.2:c.3895G>T
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XP_011529151.2:p.Gly1299Cys
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XM_017029259.2:c.3886G>T
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XP_016884748.1:p.Gly1296Cys
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XM_017029260.1:c.3877G>T
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XP_016884749.1:p.Gly1293Cys
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XM_017029261.1:c.3895G>T
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XP_016884750.1:p.Gly1299Cys
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XM_017029263.2:c.2215G>T
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XP_016884752.1:p.Gly739Cys
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NM_000495.5:c.3862G>T
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NP_000486.1:p.Gly1288Cys
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NM_033380.3:c.3880G>T
MANE Select
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NP_203699.1:p.Gly1294Cys
|
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