ENST00000284885.8:c.2627A=
MANE Select
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ENSP00000284885.3:p.Asp876=
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|
ENST00000284885.7:c.2627A=
|
ENSP00000284885.3:p.Asp876=
|
|
NM_002772.2:c.2627A=
|
NP_002763.2:p.Asp876=
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|
XM_011529654.1:c.2762A=
|
XP_011527956.1:p.Asp921=
|
|
XM_011529655.1:c.2762A=
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XP_011527957.1:p.Asp921=
|
|
XM_011529656.1:c.2762A=
|
XP_011527958.1:p.Asp921=
|
|
XM_011529657.1:c.2717A=
|
XP_011527959.1:p.Asp906=
|
|
XM_011529658.1:c.2681A=
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XP_011527960.1:p.Asp894=
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|
XM_011529659.1:c.2672A=
|
XP_011527961.1:p.Asp891=
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|
XM_011529654.2:c.2762A=
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XP_011527956.1:p.Asp921=
|
|
XM_011529656.2:c.2762A=
|
XP_011527958.1:p.Asp921=
|
|
XM_011529657.2:c.2717A=
|
XP_011527959.1:p.Asp906=
|
|
XM_011529658.2:c.2681A=
|
XP_011527960.1:p.Asp894=
|
|
NM_002772.3:c.2627A=
MANE Select
|
NP_002763.3:p.Asp876=
|
|