ENST00000328300.11:c.4199G>T
MANE Select
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ENSP00000331902.7:p.Gly1400Val
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ENST00000361603.7:c.4181G>T
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ENSP00000354505.2:p.Gly1394Val
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ENST00000510690.2:n.693G>T
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ENST00000328300.10:c.4199G>T
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ENSP00000331902.6:p.Gly1400Val
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ENST00000361603.6:c.4181G>T
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ENSP00000354505.2:p.Gly1394Val
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ENST00000489230.1:n.602G>T
|
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NM_000495.4:c.4181G>T
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NP_000486.1:p.Gly1394Val
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NM_033380.2:c.4199G>T
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NP_203699.1:p.Gly1400Val
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XM_005262070.2:c.4190G>T
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XP_005262127.1:p.Gly1397Val
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XM_006724616.2:c.4199G>T
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XP_006724679.1:p.Gly1400Val
|
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XM_011530849.1:c.3875G>T
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XP_011529151.1:p.Gly1292Val
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XM_011530851.1:c.1772G>T
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XP_011529153.1:p.Gly591Val
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XM_011530849.2:c.4214G>T
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XP_011529151.2:p.Gly1405Val
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XM_017029259.2:c.4205G>T
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XP_016884748.1:p.Gly1402Val
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XM_017029260.1:c.4196G>T
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XP_016884749.1:p.Gly1399Val
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XM_017029263.2:c.2534G>T
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XP_016884752.1:p.Gly845Val
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NM_000495.5:c.4181G>T
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NP_000486.1:p.Gly1394Val
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NM_033380.3:c.4199G>T
MANE Select
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NP_203699.1:p.Gly1400Val
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