ENST00000295754.10:c.695C>G
MANE Select
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ENSP00000295754.5:p.Ala232Gly
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ENST00000672866.1:n.2291C>G
|
|
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ENST00000295754.9:c.695C>G
|
ENSP00000295754.5:p.Ala232Gly
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ENST00000359013.4:c.770C>G
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ENSP00000351905.4:p.Ala257Gly
|
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NM_001024847.2:c.770C>G , LRG_779t1:c.770C>G
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NP_001020018.1:p.Ala257Gly
|
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NM_003242.5:c.695C>G
|
NP_003233.4:p.Ala232Gly
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XM_011534043.1:c.722C>G
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XP_011532345.1:p.Ala241Gly
|
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XM_011534044.1:c.647C>G
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XP_011532346.1:p.Ala216Gly
|
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XM_011534045.1:c.590C>G
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XP_011532347.1:p.Ala197Gly
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XM_011534043.2:c.722C>G
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XP_011532345.1:p.Ala241Gly
|
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XM_011534045.3:c.590C>G
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XP_011532347.1:p.Ala197Gly
|
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XM_017007106.1:c.590C>G
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XP_016862595.1:p.Ala197Gly
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NM_003242.6:c.695C>G
MANE Select
|
NP_003233.4:p.Ala232Gly
|
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