ENST00000234071.8:c.992A=
MANE Select
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ENSP00000234071.4:p.Asn331=
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ENST00000234071.7:c.992A=
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ENSP00000234071.3:p.Asn331=
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|
ENST00000402125.2:c.316A=
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|
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ENST00000409048.1:c.1094A=
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ENSP00000386679.1:p.Asn365=
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|
NM_000312.3:c.992A= , LRG_599t1:c.992A=
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NP_000303.1:p.Asn331=
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|
XM_005263715.3:c.1175A=
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XP_005263772.1:p.Asn392=
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XM_005263716.3:c.1157A=
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XP_005263773.1:p.Asn386=
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XM_005263717.3:c.1055A=
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XP_005263774.1:p.Asn352=
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|
XR_923313.1:n.1332-288T=
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|
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XM_005263717.4:c.1055A=
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XP_005263774.1:p.Asn352=
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|
XM_017004505.1:c.1235A=
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XP_016859994.1:p.Asn412=
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|
XM_024453002.1:c.1337A=
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XP_024308770.1:p.Asn446=
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|
XM_024453003.1:c.1277A=
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XP_024308771.1:p.Asn426=
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|
XM_024453004.1:c.1175A=
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XP_024308772.1:p.Asn392=
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|
XM_024453005.1:c.1157A=
|
XP_024308773.1:p.Asn386=
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|
XM_024453006.1:c.1094A=
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XP_024308774.1:p.Asn365=
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|
XR_001739705.1:n.3607-288T=
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|
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XR_923313.2:n.4043-288T=
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|
|
NM_000312.4:c.992A=
MANE Select
|
NP_000303.1:p.Asn331=
|
|
NM_001375602.1:c.1175A=
|
NP_001362531.1:p.Asn392=
|
|
NM_001375603.1:c.1157A=
|
NP_001362532.1:p.Asn386=
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|
NM_001375604.1:c.1055A=
|
NP_001362533.1:p.Asn352=
|
|
NM_001375605.1:c.1094A=
|
NP_001362534.1:p.Asn365=
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|
NM_001375606.1:c.1160A=
|
NP_001362535.1:p.Asn387=
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|
NM_001375607.1:c.1178A=
|
NP_001362536.1:p.Asn393=
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|
NM_001375608.1:c.935A=
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NP_001362537.1:p.Asn312=
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|
NM_001375609.1:c.968A=
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NP_001362538.1:p.Asn323=
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|
NM_001375610.1:c.986A=
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NP_001362539.1:p.Asn329=
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|
NM_001375611.1:c.992A=
|
NP_001362540.1:p.Asn331=
|
|
NM_001375613.1:c.992A=
|
NP_001362542.1:p.Asn331=
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