ENST00000295754.10:c.1394G>T
MANE Select
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ENSP00000295754.5:p.Gly465Val
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ENST00000672866.1:n.2990G>T
|
|
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ENST00000673203.1:n.272G>T
|
|
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ENST00000295754.9:c.1394G>T
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ENSP00000295754.5:p.Gly465Val
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ENST00000359013.4:c.1469G>T
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ENSP00000351905.4:p.Gly490Val
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NM_001024847.2:c.1469G>T , LRG_779t1:c.1469G>T
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NP_001020018.1:p.Gly490Val
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NM_003242.5:c.1394G>T
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NP_003233.4:p.Gly465Val
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XM_011534043.1:c.1421G>T
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XP_011532345.1:p.Gly474Val
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XM_011534044.1:c.1346G>T
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XP_011532346.1:p.Gly449Val
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XM_011534045.1:c.1289G>T
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XP_011532347.1:p.Gly430Val
|
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XM_011534043.2:c.1421G>T
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XP_011532345.1:p.Gly474Val
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XM_011534045.3:c.1289G>T
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XP_011532347.1:p.Gly430Val
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XM_017007106.1:c.1289G>T
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XP_016862595.1:p.Gly430Val
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NM_003242.6:c.1394G>T
MANE Select
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NP_003233.4:p.Gly465Val
|
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