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ENST00000234071.8:c.1166del
MANE Select
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ENSP00000234071.4:p.Gly389AlafsTer?
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ENST00000234071.7:c.1166del
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ENSP00000234071.3:p.Gly389AlafsTer?
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ENST00000402125.2:c.490del
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ENST00000409048.1:c.1268del
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ENSP00000386679.1:p.Gly423AlafsTer?
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NM_000312.3:c.1166del , LRG_599t1:c.1166del
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NP_000303.1:p.Gly389AlafsTer?
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XM_005263715.3:c.1349del
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XP_005263772.1:p.Gly450AlafsTer?
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XM_005263716.3:c.1331del
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XP_005263773.1:p.Gly444AlafsTer?
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XM_005263717.3:c.1229del
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XP_005263774.1:p.Gly410AlafsTer?
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XR_923313.1:n.1332-460del
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XM_005263717.4:c.1229del
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XP_005263774.1:p.Gly410AlafsTer?
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XM_017004505.1:c.1409del
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XP_016859994.1:p.Gly470AlafsTer?
|
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XM_024453002.1:c.1511del
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XP_024308770.1:p.Gly504AlafsTer?
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XM_024453003.1:c.1451del
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XP_024308771.1:p.Gly484AlafsTer?
|
|
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XM_024453004.1:c.1349del
|
XP_024308772.1:p.Gly450AlafsTer?
|
|
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XM_024453005.1:c.1331del
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XP_024308773.1:p.Gly444AlafsTer?
|
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XM_024453006.1:c.1268del
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XP_024308774.1:p.Gly423AlafsTer?
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XR_001739705.1:n.3607-460del
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XR_923313.2:n.4043-460del
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NM_000312.4:c.1166del
MANE Select
|
NP_000303.1:p.Gly389AlafsTer?
|
|
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NM_001375602.1:c.1349del
|
NP_001362531.1:p.Gly450AlafsTer?
|
|
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NM_001375603.1:c.1331del
|
NP_001362532.1:p.Gly444AlafsTer?
|
|
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NM_001375604.1:c.1229del
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NP_001362533.1:p.Gly410AlafsTer?
|
|
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NM_001375605.1:c.1268del
|
NP_001362534.1:p.Gly423AlafsTer?
|
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NM_001375606.1:c.1334del
|
NP_001362535.1:p.Gly445AlafsTer?
|
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NM_001375607.1:c.1352del
|
NP_001362536.1:p.Gly451AlafsTer?
|
|
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NM_001375608.1:c.1109del
|
NP_001362537.1:p.Gly370AlafsTer?
|
|
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NM_001375609.1:c.1142del
|
NP_001362538.1:p.Gly381AlafsTer?
|
|
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NM_001375610.1:c.1160del
|
NP_001362539.1:p.Gly387AlafsTer?
|
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NM_001375611.1:c.1166del
|
NP_001362540.1:p.Gly389AlafsTer?
|
|
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NM_001375613.1:c.1166del
|
NP_001362542.1:p.Gly389AlafsTer?
|
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