ENST00000328300.11:c.4371T>C
MANE Select
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ENSP00000331902.7:p.Gly1457=
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ENST00000361603.7:c.4353T>C
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ENSP00000354505.2:p.Gly1451=
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ENST00000510690.2:n.865T>C
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ENST00000328300.10:c.4371T>C
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ENSP00000331902.6:p.Gly1457=
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ENST00000361603.6:c.4353T>C
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ENSP00000354505.2:p.Gly1451=
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ENST00000515658.1:c.167T>C
|
|
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NM_000495.4:c.4353T>C
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NP_000486.1:p.Gly1451=
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NM_033380.2:c.4371T>C
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NP_203699.1:p.Gly1457=
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XM_005262070.2:c.4362T>C
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XP_005262127.1:p.Gly1454=
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XM_006724616.2:c.4371T>C
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XP_006724679.1:p.Gly1457=
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XM_011530849.1:c.4047T>C
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XP_011529151.1:p.Gly1349=
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XM_011530851.1:c.1944T>C
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XP_011529153.1:p.Gly648=
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XM_011530849.2:c.4386T>C
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XP_011529151.2:p.Gly1462=
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XM_017029259.2:c.4377T>C
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XP_016884748.1:p.Gly1459=
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XM_017029260.1:c.4368T>C
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XP_016884749.1:p.Gly1456=
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XM_017029263.2:c.2706T>C
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XP_016884752.1:p.Gly902=
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NM_000495.5:c.4353T>C
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NP_000486.1:p.Gly1451=
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NM_033380.3:c.4371T>C
MANE Select
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NP_203699.1:p.Gly1457=
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