ENST00000393716.8:c.107G>T
MANE Select
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ENSP00000377319.3:p.Gly36Val
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ENST00000466380.6:c.107G>T
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ENSP00000420297.2:p.Gly36Val
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ENST00000648112.1:c.*130G>T
|
ENSP00000497876.1:n.*130G>T
|
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ENST00000337940.4:c.224G>T
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ENSP00000336528.4:p.Gly75Val
|
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ENST00000393716.6:c.107G>T
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ENSP00000377319.2:p.Gly36Val
|
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ENST00000466380.5:c.107G>T
|
ENSP00000420297.1:p.Gly36Val
|
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ENST00000474090.1:n.395G>T
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|
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NM_003889.3:c.107G>T
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NP_003880.3:p.Gly36Val
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NM_022002.2:c.224G>T
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NP_071285.1:p.Gly75Val
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NM_033013.2:c.107G>T
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NP_148934.1:p.Gly36Val
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|
NM_003889.4:c.107G>T
MANE Select
|
NP_003880.3:p.Gly36Val
|
|
NM_022002.3:c.224G>T
|
NP_071285.1:p.Gly75Val
|
|
NM_033013.3:c.107G>T
|
NP_148934.1:p.Gly36Val
|
|