ENST00000328300.11:c.3836G>T
MANE Select
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ENSP00000331902.7:p.Gly1279Val
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ENST00000361603.7:c.3818G>T
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ENSP00000354505.2:p.Gly1273Val
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ENST00000510690.2:n.330G>T
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ENST00000328300.10:c.3836G>T
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ENSP00000331902.6:p.Gly1279Val
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ENST00000361603.6:c.3818G>T
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ENSP00000354505.2:p.Gly1273Val
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ENST00000489230.1:n.239G>T
|
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ENST00000510690.1:n.330G>T
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NM_000495.4:c.3818G>T
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NP_000486.1:p.Gly1273Val
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NM_033380.2:c.3836G>T
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NP_203699.1:p.Gly1279Val
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XM_005262070.2:c.3827G>T
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XP_005262127.1:p.Gly1276Val
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XM_006724616.2:c.3836G>T
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XP_006724679.1:p.Gly1279Val
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XM_011530849.1:c.3512G>T
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XP_011529151.1:p.Gly1171Val
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XM_011530851.1:c.1409G>T
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XP_011529153.1:p.Gly470Val
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XM_011530849.2:c.3851G>T
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XP_011529151.2:p.Gly1284Val
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XM_017029259.2:c.3842G>T
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XP_016884748.1:p.Gly1281Val
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XM_017029260.1:c.3833G>T
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XP_016884749.1:p.Gly1278Val
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XM_017029261.1:c.3851G>T
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XP_016884750.1:p.Gly1284Val
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XM_017029263.2:c.2171G>T
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XP_016884752.1:p.Gly724Val
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NM_000495.5:c.3818G>T
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NP_000486.1:p.Gly1273Val
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NM_033380.3:c.3836G>T
MANE Select
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NP_203699.1:p.Gly1279Val
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