ENST00000328300.11:c.4037T>G
MANE Select
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ENSP00000331902.7:p.Val1346Gly
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ENST00000361603.7:c.4019T>G
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ENSP00000354505.2:p.Val1340Gly
|
|
ENST00000510690.2:n.531T>G
|
|
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ENST00000328300.10:c.4037T>G
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ENSP00000331902.6:p.Val1346Gly
|
|
ENST00000361603.6:c.4019T>G
|
ENSP00000354505.2:p.Val1340Gly
|
|
ENST00000489230.1:n.440T>G
|
|
|
NM_000495.4:c.4019T>G
|
NP_000486.1:p.Val1340Gly
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NM_033380.2:c.4037T>G
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NP_203699.1:p.Val1346Gly
|
|
XM_005262070.2:c.4028T>G
|
XP_005262127.1:p.Val1343Gly
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XM_006724616.2:c.4037T>G
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XP_006724679.1:p.Val1346Gly
|
|
XM_011530849.1:c.3713T>G
|
XP_011529151.1:p.Val1238Gly
|
|
XM_011530851.1:c.1610T>G
|
XP_011529153.1:p.Val537Gly
|
|
XM_011530849.2:c.4052T>G
|
XP_011529151.2:p.Val1351Gly
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XM_017029259.2:c.4043T>G
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XP_016884748.1:p.Val1348Gly
|
|
XM_017029260.1:c.4034T>G
|
XP_016884749.1:p.Val1345Gly
|
|
XM_017029263.2:c.2372T>G
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XP_016884752.1:p.Val791Gly
|
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NM_000495.5:c.4019T>G
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NP_000486.1:p.Val1340Gly
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NM_033380.3:c.4037T>G
MANE Select
|
NP_203699.1:p.Val1346Gly
|
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