ENST00000234071.8:c.1195G>T
MANE Select
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ENSP00000234071.4:p.Glu399Ter
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ENST00000234071.7:c.1195G>T
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ENSP00000234071.3:p.Glu399Ter
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ENST00000402125.2:c.519G>T
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|
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ENST00000409048.1:c.1297G>T
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ENSP00000386679.1:p.Glu433Ter
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NM_000312.3:c.1195G>T , LRG_599t1:c.1195G>T
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NP_000303.1:p.Glu399Ter
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XM_005263715.3:c.1378G>T
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XP_005263772.1:p.Glu460Ter
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XM_005263716.3:c.1360G>T
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XP_005263773.1:p.Glu454Ter
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XM_005263717.3:c.1258G>T
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XP_005263774.1:p.Glu420Ter
|
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XR_923313.1:n.1332-491C>A
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XM_005263717.4:c.1258G>T
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XP_005263774.1:p.Glu420Ter
|
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XM_017004505.1:c.1438G>T
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XP_016859994.1:p.Glu480Ter
|
|
XM_024453002.1:c.1540G>T
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XP_024308770.1:p.Glu514Ter
|
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XM_024453003.1:c.1480G>T
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XP_024308771.1:p.Glu494Ter
|
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XM_024453004.1:c.1378G>T
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XP_024308772.1:p.Glu460Ter
|
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XM_024453005.1:c.1360G>T
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XP_024308773.1:p.Glu454Ter
|
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XM_024453006.1:c.1297G>T
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XP_024308774.1:p.Glu433Ter
|
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XR_001739705.1:n.3607-491C>A
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XR_923313.2:n.4043-491C>A
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NM_000312.4:c.1195G>T
MANE Select
|
NP_000303.1:p.Glu399Ter
|
|
NM_001375602.1:c.1378G>T
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NP_001362531.1:p.Glu460Ter
|
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NM_001375603.1:c.1360G>T
|
NP_001362532.1:p.Glu454Ter
|
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NM_001375604.1:c.1258G>T
|
NP_001362533.1:p.Glu420Ter
|
|
NM_001375605.1:c.1297G>T
|
NP_001362534.1:p.Glu433Ter
|
|
NM_001375606.1:c.1363G>T
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NP_001362535.1:p.Glu455Ter
|
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NM_001375607.1:c.1381G>T
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NP_001362536.1:p.Glu461Ter
|
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NM_001375608.1:c.1138G>T
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NP_001362537.1:p.Glu380Ter
|
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NM_001375609.1:c.1171G>T
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NP_001362538.1:p.Glu391Ter
|
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NM_001375610.1:c.1189G>T
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NP_001362539.1:p.Glu397Ter
|
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NM_001375611.1:c.1195G>T
|
NP_001362540.1:p.Glu399Ter
|
|
NM_001375613.1:c.1195G>T
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NP_001362542.1:p.Glu399Ter
|
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