ENST00000234071.8:c.1261A=
MANE Select
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ENSP00000234071.4:p.Ser421=
|
|
ENST00000234071.7:c.1261A=
|
ENSP00000234071.3:p.Ser421=
|
|
ENST00000402125.2:c.585A=
|
|
|
ENST00000409048.1:c.1363A=
|
ENSP00000386679.1:p.Ser455=
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|
NM_000312.3:c.1261A= , LRG_599t1:c.1261A=
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NP_000303.1:p.Ser421=
|
|
XM_005263715.3:c.1444A=
|
XP_005263772.1:p.Ser482=
|
|
XM_005263716.3:c.1426A=
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XP_005263773.1:p.Ser476=
|
|
XM_005263717.3:c.1324A=
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XP_005263774.1:p.Ser442=
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|
XR_923313.1:n.1332-557T=
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|
|
XM_005263717.4:c.1324A=
|
XP_005263774.1:p.Ser442=
|
|
XM_017004505.1:c.1504A=
|
XP_016859994.1:p.Ser502=
|
|
XM_024453002.1:c.1606A=
|
XP_024308770.1:p.Ser536=
|
|
XM_024453003.1:c.1546A=
|
XP_024308771.1:p.Ser516=
|
|
XM_024453004.1:c.1444A=
|
XP_024308772.1:p.Ser482=
|
|
XM_024453005.1:c.1426A=
|
XP_024308773.1:p.Ser476=
|
|
XM_024453006.1:c.1363A=
|
XP_024308774.1:p.Ser455=
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|
XR_001739705.1:n.3607-557T=
|
|
|
XR_923313.2:n.4043-557T=
|
|
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NM_000312.4:c.1261A=
MANE Select
|
NP_000303.1:p.Ser421=
|
|
NM_001375602.1:c.1444A=
|
NP_001362531.1:p.Ser482=
|
|
NM_001375603.1:c.1426A=
|
NP_001362532.1:p.Ser476=
|
|
NM_001375604.1:c.1324A=
|
NP_001362533.1:p.Ser442=
|
|
NM_001375605.1:c.1363A=
|
NP_001362534.1:p.Ser455=
|
|
NM_001375606.1:c.1429A=
|
NP_001362535.1:p.Ser477=
|
|
NM_001375607.1:c.1447A=
|
NP_001362536.1:p.Ser483=
|
|
NM_001375608.1:c.1204A=
|
NP_001362537.1:p.Ser402=
|
|
NM_001375609.1:c.1237A=
|
NP_001362538.1:p.Ser413=
|
|
NM_001375610.1:c.1255A=
|
NP_001362539.1:p.Ser419=
|
|
NM_001375611.1:c.1261A=
|
NP_001362540.1:p.Ser421=
|
|
NM_001375613.1:c.1261A=
|
NP_001362542.1:p.Ser421=
|
|