ENST00000328300.11:c.4096G>A
MANE Select
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ENSP00000331902.7:p.Gly1366Arg
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ENST00000361603.7:c.4078G>A
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ENSP00000354505.2:p.Gly1360Arg
|
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ENST00000510690.2:n.590G>A
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ENST00000328300.10:c.4096G>A
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ENSP00000331902.6:p.Gly1366Arg
|
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ENST00000361603.6:c.4078G>A
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ENSP00000354505.2:p.Gly1360Arg
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ENST00000489230.1:n.499G>A
|
|
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NM_000495.4:c.4078G>A
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NP_000486.1:p.Gly1360Arg
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NM_033380.2:c.4096G>A
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NP_203699.1:p.Gly1366Arg
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XM_005262070.2:c.4087G>A
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XP_005262127.1:p.Gly1363Arg
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XM_006724616.2:c.4096G>A
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XP_006724679.1:p.Gly1366Arg
|
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XM_011530849.1:c.3772G>A
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XP_011529151.1:p.Gly1258Arg
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XM_011530851.1:c.1669G>A
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XP_011529153.1:p.Gly557Arg
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XM_011530849.2:c.4111G>A
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XP_011529151.2:p.Gly1371Arg
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XM_017029259.2:c.4102G>A
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XP_016884748.1:p.Gly1368Arg
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XM_017029260.1:c.4093G>A
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XP_016884749.1:p.Gly1365Arg
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XM_017029263.2:c.2431G>A
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XP_016884752.1:p.Gly811Arg
|
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NM_000495.5:c.4078G>A
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NP_000486.1:p.Gly1360Arg
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NM_033380.3:c.4096G>A
MANE Select
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NP_203699.1:p.Gly1366Arg
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