ENST00000234071.8:c.1114G>A
MANE Select
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ENSP00000234071.4:p.Glu372Lys
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ENST00000234071.7:c.1114G>A
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ENSP00000234071.3:p.Glu372Lys
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ENST00000402125.2:c.438G>A
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|
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ENST00000409048.1:c.1216G>A
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ENSP00000386679.1:p.Glu406Lys
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NM_000312.3:c.1114G>A , LRG_599t1:c.1114G>A
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NP_000303.1:p.Glu372Lys
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XM_005263715.3:c.1297G>A
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XP_005263772.1:p.Glu433Lys
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XM_005263716.3:c.1279G>A
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XP_005263773.1:p.Glu427Lys
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XM_005263717.3:c.1177G>A
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XP_005263774.1:p.Glu393Lys
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XR_923313.1:n.1332-410C>T
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|
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XM_005263717.4:c.1177G>A
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XP_005263774.1:p.Glu393Lys
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XM_017004505.1:c.1357G>A
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XP_016859994.1:p.Glu453Lys
|
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XM_024453002.1:c.1459G>A
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XP_024308770.1:p.Glu487Lys
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XM_024453003.1:c.1399G>A
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XP_024308771.1:p.Glu467Lys
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XM_024453004.1:c.1297G>A
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XP_024308772.1:p.Glu433Lys
|
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XM_024453005.1:c.1279G>A
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XP_024308773.1:p.Glu427Lys
|
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XM_024453006.1:c.1216G>A
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XP_024308774.1:p.Glu406Lys
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XR_001739705.1:n.3607-410C>T
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XR_923313.2:n.4043-410C>T
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NM_000312.4:c.1114G>A
MANE Select
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NP_000303.1:p.Glu372Lys
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NM_001375602.1:c.1297G>A
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NP_001362531.1:p.Glu433Lys
|
|
NM_001375603.1:c.1279G>A
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NP_001362532.1:p.Glu427Lys
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NM_001375604.1:c.1177G>A
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NP_001362533.1:p.Glu393Lys
|
|
NM_001375605.1:c.1216G>A
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NP_001362534.1:p.Glu406Lys
|
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NM_001375606.1:c.1282G>A
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NP_001362535.1:p.Glu428Lys
|
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NM_001375607.1:c.1300G>A
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NP_001362536.1:p.Glu434Lys
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NM_001375608.1:c.1057G>A
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NP_001362537.1:p.Glu353Lys
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NM_001375609.1:c.1090G>A
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NP_001362538.1:p.Glu364Lys
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NM_001375610.1:c.1108G>A
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NP_001362539.1:p.Glu370Lys
|
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NM_001375611.1:c.1114G>A
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NP_001362540.1:p.Glu372Lys
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NM_001375613.1:c.1114G>A
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NP_001362542.1:p.Glu372Lys
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