ENST00000328300.11:c.4097G>A
MANE Select
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ENSP00000331902.7:p.Gly1366Glu
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ENST00000361603.7:c.4079G>A
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ENSP00000354505.2:p.Gly1360Glu
|
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ENST00000510690.2:n.591G>A
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ENST00000328300.10:c.4097G>A
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ENSP00000331902.6:p.Gly1366Glu
|
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ENST00000361603.6:c.4079G>A
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ENSP00000354505.2:p.Gly1360Glu
|
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ENST00000489230.1:n.500G>A
|
|
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NM_000495.4:c.4079G>A
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NP_000486.1:p.Gly1360Glu
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NM_033380.2:c.4097G>A
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NP_203699.1:p.Gly1366Glu
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XM_005262070.2:c.4088G>A
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XP_005262127.1:p.Gly1363Glu
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XM_006724616.2:c.4097G>A
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XP_006724679.1:p.Gly1366Glu
|
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XM_011530849.1:c.3773G>A
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XP_011529151.1:p.Gly1258Glu
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XM_011530851.1:c.1670G>A
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XP_011529153.1:p.Gly557Glu
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XM_011530849.2:c.4112G>A
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XP_011529151.2:p.Gly1371Glu
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XM_017029259.2:c.4103G>A
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XP_016884748.1:p.Gly1368Glu
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XM_017029260.1:c.4094G>A
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XP_016884749.1:p.Gly1365Glu
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XM_017029263.2:c.2432G>A
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XP_016884752.1:p.Gly811Glu
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NM_000495.5:c.4079G>A
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NP_000486.1:p.Gly1360Glu
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NM_033380.3:c.4097G>A
MANE Select
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NP_203699.1:p.Gly1366Glu
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