ENST00000650516.2:c.665G>C
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ENSP00000498052.2:p.Gly222Ala
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ENST00000343257.7:c.665G>C
MANE Select
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ENSP00000339867.2:p.Gly222Ala
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ENST00000432192.6:c.433G>C
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ENST00000455478.6:c.119G>C
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ENSP00000400027.2:p.Gly40Ala
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ENST00000650516.1:c.665G>C
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ENSP00000498052.1:p.Gly222Ala
|
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ENST00000343257.6:c.665G>C
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ENSP00000339867.2:p.Gly222Ala
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ENST00000432192.5:c.123G>C
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ENST00000455478.5:c.123G>C
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ENST00000495612.1:n.123G>C
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NM_000083.2:c.665G>C
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NP_000074.2:p.Gly222Ala
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NR_046453.1:n.752G>C
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XM_011515781.1:c.665G>C
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XP_011514083.1:p.Gly222Ala
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XM_017011739.1:c.372G>C
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XP_016867228.1:p.Gly124=
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XM_017011740.1:c.372G>C
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XP_016867229.1:p.Gly124=
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NM_000083.3:c.665G>C
MANE Select
|
NP_000074.3:p.Gly222Ala
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NR_046453.2:n.767G>C
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