ENST00000328300.11:c.2623G>T
MANE Select
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ENSP00000331902.7:p.Gly875Ter
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ENST00000361603.7:c.2623G>T
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ENSP00000354505.2:p.Gly875Ter
|
|
ENST00000328300.10:c.2623G>T
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ENSP00000331902.6:p.Gly875Ter
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ENST00000361603.6:c.2623G>T
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ENSP00000354505.2:p.Gly875Ter
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ENST00000483338.1:n.2079G>T
|
|
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NM_000495.4:c.2623G>T
|
NP_000486.1:p.Gly875Ter
|
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NM_033380.2:c.2623G>T
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NP_203699.1:p.Gly875Ter
|
|
XM_005262070.2:c.2623G>T
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XP_005262127.1:p.Gly875Ter
|
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XM_005262072.3:c.2623G>T
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XP_005262129.1:p.Gly875Ter
|
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XM_006724616.2:c.2623G>T
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XP_006724679.1:p.Gly875Ter
|
|
XM_011530849.1:c.2299G>T
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XP_011529151.1:p.Gly767Ter
|
|
XM_011530850.1:c.2623G>T
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XP_011529152.1:p.Gly875Ter
|
|
XM_011530851.1:c.196G>T
|
XP_011529153.1:p.Gly66Ter
|
|
XM_011530849.2:c.2638G>T
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XP_011529151.2:p.Gly880Ter
|
|
XM_017029259.2:c.2638G>T
|
XP_016884748.1:p.Gly880Ter
|
|
XM_017029260.1:c.2638G>T
|
XP_016884749.1:p.Gly880Ter
|
|
XM_017029261.1:c.2638G>T
|
XP_016884750.1:p.Gly880Ter
|
|
XM_017029262.2:c.2638G>T
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XP_016884751.1:p.Gly880Ter
|
|
XM_017029263.2:c.958G>T
|
XP_016884752.1:p.Gly320Ter
|
|
NM_000495.5:c.2623G>T
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NP_000486.1:p.Gly875Ter
|
|
NM_033380.3:c.2623G>T
MANE Select
|
NP_203699.1:p.Gly875Ter
|
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