ENST00000355773.6:c.1319G>T
MANE Select
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ENSP00000348019.5:p.Gly440Val
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ENST00000355773.5:c.1319G>T
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ENSP00000348019.5:p.Gly440Val
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NM_012434.4:c.1319G>T
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NP_036566.1:p.Gly440Val
|
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XM_005248710.2:c.1268G>T
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XP_005248767.1:p.Gly423Val
|
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XM_005248711.1:c.1121G>T
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XP_005248768.1:p.Gly374Val
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XM_011535750.1:c.1171G>T
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XP_011534052.1:p.Gly391Cys
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NM_012434.5:c.1319G>T
MANE Select
|
NP_036566.1:p.Gly440Val
|
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NM_001382629.1:c.1088G>T
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NP_001369558.1:p.Gly363Val
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NM_001382630.1:c.1260-5168G>T
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NP_001369559.1:n.1260-5168G>T
|
|
NM_001382631.1:c.1340G>T
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NP_001369560.1:p.Gly447Val
|
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NM_001382632.1:c.1232G>T
|
NP_001369561.1:p.Gly411Val
|
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NM_001382633.1:c.1319G>T
|
NP_001369562.1:p.Gly440Val
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NM_001382634.1:c.1160G>T
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NP_001369563.1:p.Gly387Val
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NM_001382635.1:c.1316G>T
|
NP_001369564.1:p.Gly439Val
|
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NM_001382636.1:c.1001G>T
|
NP_001369565.1:p.Gly334Val
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