ENST00000684241.1:n.1753C>G
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ENST00000262186.10:c.920C>G
MANE Select
|
ENSP00000262186.5:p.Ala307Gly
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ENST00000262186.9:c.920C>G
|
ENSP00000262186.5:p.Ala307Gly
|
|
ENST00000430723.4:c.572C>G
|
ENSP00000387657.4:p.Ala191Gly
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ENST00000532957.5:n.1143C>G
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NM_000238.3:c.920C>G , LRG_288t1:c.920C>G
|
NP_000229.1:p.Ala307Gly
|
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NM_172056.2:c.920C>G , LRG_288t2:c.920C>G
|
NP_742053.1:p.Ala307Gly
|
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XM_011516185.1:c.620C>G
|
XP_011514487.1:p.Ala207Gly
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XM_011516186.1:c.920C>G
|
XP_011514488.1:p.Ala307Gly
|
|
XM_011516185.2:c.620C>G
|
XP_011514487.1:p.Ala207Gly
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XM_011516186.3:c.920C>G
|
XP_011514488.1:p.Ala307Gly
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XM_017012195.1:c.770C>G
|
XP_016867684.1:p.Ala257Gly
|
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XM_017012196.1:c.743C>G
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XP_016867685.1:p.Ala248Gly
|
|
NM_000238.4:c.920C>G
MANE Select
|
NP_000229.1:p.Ala307Gly
|
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