ENST00000328300.11:c.4180G>A
MANE Select
|
ENSP00000331902.7:p.Gly1394Ser
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ENST00000361603.7:c.4162G>A
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ENSP00000354505.2:p.Gly1388Ser
|
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ENST00000510690.2:n.674G>A
|
|
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ENST00000328300.10:c.4180G>A
|
ENSP00000331902.6:p.Gly1394Ser
|
|
ENST00000361603.6:c.4162G>A
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ENSP00000354505.2:p.Gly1388Ser
|
|
ENST00000489230.1:n.583G>A
|
|
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NM_000495.4:c.4162G>A
|
NP_000486.1:p.Gly1388Ser
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NM_033380.2:c.4180G>A
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NP_203699.1:p.Gly1394Ser
|
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XM_005262070.2:c.4171G>A
|
XP_005262127.1:p.Gly1391Ser
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XM_006724616.2:c.4180G>A
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XP_006724679.1:p.Gly1394Ser
|
|
XM_011530849.1:c.3856G>A
|
XP_011529151.1:p.Gly1286Ser
|
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XM_011530851.1:c.1753G>A
|
XP_011529153.1:p.Gly585Ser
|
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XM_011530849.2:c.4195G>A
|
XP_011529151.2:p.Gly1399Ser
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XM_017029259.2:c.4186G>A
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XP_016884748.1:p.Gly1396Ser
|
|
XM_017029260.1:c.4177G>A
|
XP_016884749.1:p.Gly1393Ser
|
|
XM_017029263.2:c.2515G>A
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XP_016884752.1:p.Gly839Ser
|
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NM_000495.5:c.4162G>A
|
NP_000486.1:p.Gly1388Ser
|
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NM_033380.3:c.4180G>A
MANE Select
|
NP_203699.1:p.Gly1394Ser
|
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