ENST00000328300.11:c.4080T>A
MANE Select
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ENSP00000331902.7:p.Gly1360=
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ENST00000361603.7:c.4062T>A
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ENSP00000354505.2:p.Gly1354=
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ENST00000510690.2:n.574T>A
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ENST00000328300.10:c.4080T>A
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ENSP00000331902.6:p.Gly1360=
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ENST00000361603.6:c.4062T>A
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ENSP00000354505.2:p.Gly1354=
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ENST00000489230.1:n.483T>A
|
|
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NM_000495.4:c.4062T>A
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NP_000486.1:p.Gly1354=
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NM_033380.2:c.4080T>A
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NP_203699.1:p.Gly1360=
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XM_005262070.2:c.4071T>A
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XP_005262127.1:p.Gly1357=
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XM_006724616.2:c.4080T>A
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XP_006724679.1:p.Gly1360=
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XM_011530849.1:c.3756T>A
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XP_011529151.1:p.Gly1252=
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XM_011530851.1:c.1653T>A
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XP_011529153.1:p.Gly551=
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XM_011530849.2:c.4095T>A
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XP_011529151.2:p.Gly1365=
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XM_017029259.2:c.4086T>A
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XP_016884748.1:p.Gly1362=
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XM_017029260.1:c.4077T>A
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XP_016884749.1:p.Gly1359=
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XM_017029263.2:c.2415T>A
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XP_016884752.1:p.Gly805=
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NM_000495.5:c.4062T>A
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NP_000486.1:p.Gly1354=
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NM_033380.3:c.4080T>A
MANE Select
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NP_203699.1:p.Gly1360=
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