ENST00000328300.11:c.3826G>A
MANE Select
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ENSP00000331902.7:p.Gly1276Ser
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ENST00000361603.7:c.3808G>A
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ENSP00000354505.2:p.Gly1270Ser
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ENST00000510690.2:n.320G>A
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|
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ENST00000328300.10:c.3826G>A
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ENSP00000331902.6:p.Gly1276Ser
|
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ENST00000361603.6:c.3808G>A
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ENSP00000354505.2:p.Gly1270Ser
|
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ENST00000489230.1:n.229G>A
|
|
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ENST00000510690.1:n.320G>A
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|
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NM_000495.4:c.3808G>A
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NP_000486.1:p.Gly1270Ser
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NM_033380.2:c.3826G>A
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NP_203699.1:p.Gly1276Ser
|
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XM_005262070.2:c.3817G>A
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XP_005262127.1:p.Gly1273Ser
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XM_006724616.2:c.3826G>A
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XP_006724679.1:p.Gly1276Ser
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XM_011530849.1:c.3502G>A
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XP_011529151.1:p.Gly1168Ser
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XM_011530851.1:c.1399G>A
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XP_011529153.1:p.Gly467Ser
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XM_011530849.2:c.3841G>A
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XP_011529151.2:p.Gly1281Ser
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XM_017029259.2:c.3832G>A
|
XP_016884748.1:p.Gly1278Ser
|
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XM_017029260.1:c.3823G>A
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XP_016884749.1:p.Gly1275Ser
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XM_017029261.1:c.3841G>A
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XP_016884750.1:p.Gly1281Ser
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XM_017029263.2:c.2161G>A
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XP_016884752.1:p.Gly721Ser
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NM_000495.5:c.3808G>A
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NP_000486.1:p.Gly1270Ser
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NM_033380.3:c.3826G>A
MANE Select
|
NP_203699.1:p.Gly1276Ser
|
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