ENST00000328300.11:c.2826T>C
MANE Select
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ENSP00000331902.7:p.Ser942=
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ENST00000361603.7:c.2826T>C
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ENSP00000354505.2:p.Ser942=
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ENST00000328300.10:c.2826T>C
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ENSP00000331902.6:p.Ser942=
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ENST00000361603.6:c.2826T>C
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ENSP00000354505.2:p.Ser942=
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ENST00000483338.1:n.2282T>C
|
|
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ENST00000505728.1:c.59T>C
|
|
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NM_000495.4:c.2826T>C
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NP_000486.1:p.Ser942=
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NM_033380.2:c.2826T>C
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NP_203699.1:p.Ser942=
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XM_005262070.2:c.2826T>C
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XP_005262127.1:p.Ser942=
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XM_005262072.3:c.2826T>C
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XP_005262129.1:p.Ser942=
|
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XM_006724616.2:c.2826T>C
|
XP_006724679.1:p.Ser942=
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XM_011530849.1:c.2502T>C
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XP_011529151.1:p.Ser834=
|
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XM_011530850.1:c.2826T>C
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XP_011529152.1:p.Ser942=
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XM_011530851.1:c.399T>C
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XP_011529153.1:p.Ser133=
|
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XM_011530849.2:c.2841T>C
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XP_011529151.2:p.Ser947=
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XM_017029259.2:c.2841T>C
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XP_016884748.1:p.Ser947=
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XM_017029260.1:c.2841T>C
|
XP_016884749.1:p.Ser947=
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XM_017029261.1:c.2841T>C
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XP_016884750.1:p.Ser947=
|
|
XM_017029262.2:c.2841T>C
|
XP_016884751.1:p.Ser947=
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XM_017029263.2:c.1161T>C
|
XP_016884752.1:p.Ser387=
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|
NM_000495.5:c.2826T>C
|
NP_000486.1:p.Ser942=
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NM_033380.3:c.2826T>C
MANE Select
|
NP_203699.1:p.Ser942=
|
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