ENST00000355773.6:c.1310G>T
MANE Select
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ENSP00000348019.5:p.Gly437Val
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ENST00000355773.5:c.1310G>T
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ENSP00000348019.5:p.Gly437Val
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NM_012434.4:c.1310G>T
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NP_036566.1:p.Gly437Val
|
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XM_005248710.2:c.1259G>T
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XP_005248767.1:p.Gly420Val
|
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XM_005248711.1:c.1112G>T
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XP_005248768.1:p.Gly371Val
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XM_011535750.1:c.1162G>T
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XP_011534052.1:p.Glu388Ter
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NM_012434.5:c.1310G>T
MANE Select
|
NP_036566.1:p.Gly437Val
|
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NM_001382629.1:c.1079G>T
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NP_001369558.1:p.Gly360Val
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NM_001382630.1:c.1260-5177G>T
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NP_001369559.1:n.1260-5177G>T
|
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NM_001382631.1:c.1331G>T
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NP_001369560.1:p.Gly444Val
|
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NM_001382632.1:c.1223G>T
|
NP_001369561.1:p.Gly408Val
|
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NM_001382633.1:c.1310G>T
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NP_001369562.1:p.Gly437Val
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NM_001382634.1:c.1151G>T
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NP_001369563.1:p.Gly384Val
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NM_001382635.1:c.1307G>T
|
NP_001369564.1:p.Gly436Val
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NM_001382636.1:c.992G>T
|
NP_001369565.1:p.Gly331Val
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