ENST00000234071.8:c.1179C>G
MANE Select
|
ENSP00000234071.4:p.Asp393Glu
|
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ENST00000234071.7:c.1179C>G
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ENSP00000234071.3:p.Asp393Glu
|
|
ENST00000402125.2:c.503C>G
|
|
|
ENST00000409048.1:c.1281C>G
|
ENSP00000386679.1:p.Asp427Glu
|
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NM_000312.3:c.1179C>G , LRG_599t1:c.1179C>G
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NP_000303.1:p.Asp393Glu
|
|
XM_005263715.3:c.1362C>G
|
XP_005263772.1:p.Asp454Glu
|
|
XM_005263716.3:c.1344C>G
|
XP_005263773.1:p.Asp448Glu
|
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XM_005263717.3:c.1242C>G
|
XP_005263774.1:p.Asp414Glu
|
|
XR_923313.1:n.1332-475G>C
|
|
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XM_005263717.4:c.1242C>G
|
XP_005263774.1:p.Asp414Glu
|
|
XM_017004505.1:c.1422C>G
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XP_016859994.1:p.Asp474Glu
|
|
XM_024453002.1:c.1524C>G
|
XP_024308770.1:p.Asp508Glu
|
|
XM_024453003.1:c.1464C>G
|
XP_024308771.1:p.Asp488Glu
|
|
XM_024453004.1:c.1362C>G
|
XP_024308772.1:p.Asp454Glu
|
|
XM_024453005.1:c.1344C>G
|
XP_024308773.1:p.Asp448Glu
|
|
XM_024453006.1:c.1281C>G
|
XP_024308774.1:p.Asp427Glu
|
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XR_001739705.1:n.3607-475G>C
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|
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XR_923313.2:n.4043-475G>C
|
|
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NM_000312.4:c.1179C>G
MANE Select
|
NP_000303.1:p.Asp393Glu
|
|
NM_001375602.1:c.1362C>G
|
NP_001362531.1:p.Asp454Glu
|
|
NM_001375603.1:c.1344C>G
|
NP_001362532.1:p.Asp448Glu
|
|
NM_001375604.1:c.1242C>G
|
NP_001362533.1:p.Asp414Glu
|
|
NM_001375605.1:c.1281C>G
|
NP_001362534.1:p.Asp427Glu
|
|
NM_001375606.1:c.1347C>G
|
NP_001362535.1:p.Asp449Glu
|
|
NM_001375607.1:c.1365C>G
|
NP_001362536.1:p.Asp455Glu
|
|
NM_001375608.1:c.1122C>G
|
NP_001362537.1:p.Asp374Glu
|
|
NM_001375609.1:c.1155C>G
|
NP_001362538.1:p.Asp385Glu
|
|
NM_001375610.1:c.1173C>G
|
NP_001362539.1:p.Asp391Glu
|
|
NM_001375611.1:c.1179C>G
|
NP_001362540.1:p.Asp393Glu
|
|
NM_001375613.1:c.1179C>G
|
NP_001362542.1:p.Asp393Glu
|
|