ENST00000295754.10:c.1242T>G
MANE Select
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ENSP00000295754.5:p.Ala414=
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ENST00000672866.1:n.2838T>G
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|
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ENST00000295754.9:c.1242T>G
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ENSP00000295754.5:p.Ala414=
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ENST00000359013.4:c.1317T>G
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ENSP00000351905.4:p.Ala439=
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NM_001024847.2:c.1317T>G , LRG_779t1:c.1317T>G
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NP_001020018.1:p.Ala439=
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NM_003242.5:c.1242T>G
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NP_003233.4:p.Ala414=
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XM_011534043.1:c.1269T>G
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XP_011532345.1:p.Ala423=
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XM_011534044.1:c.1194T>G
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XP_011532346.1:p.Ala398=
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XM_011534045.1:c.1137T>G
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XP_011532347.1:p.Ala379=
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XM_011534043.2:c.1269T>G
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XP_011532345.1:p.Ala423=
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XM_011534045.3:c.1137T>G
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XP_011532347.1:p.Ala379=
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XM_017007106.1:c.1137T>G
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XP_016862595.1:p.Ala379=
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NM_003242.6:c.1242T>G
MANE Select
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NP_003233.4:p.Ala414=
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