ENST00000684241.1:n.3811G>C
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ENST00000262186.10:c.2978G>C
MANE Select
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ENSP00000262186.5:p.Gly993Ala
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ENST00000330883.9:c.1958G>C
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ENSP00000328531.4:p.Gly653Ala
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ENST00000262186.9:c.2978G>C
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ENSP00000262186.5:p.Gly993Ala
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ENST00000330883.8:c.1958G>C
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ENSP00000328531.4:p.Gly653Ala
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NM_000238.3:c.2978G>C , LRG_288t1:c.2978G>C
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NP_000229.1:p.Gly993Ala
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NM_172057.2:c.1958G>C , LRG_288t3:c.1958G>C
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NP_742054.1:p.Gly653Ala
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XM_011516185.1:c.2678G>C
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XP_011514487.1:p.Gly893Ala
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XM_011516186.1:c.*58G>C
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XP_011514488.1:n.*58G>C
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XM_011516185.2:c.2678G>C
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XP_011514487.1:p.Gly893Ala
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XM_011516186.3:c.*58G>C
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XP_011514488.1:n.*58G>C
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XM_017012195.1:c.2828G>C
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XP_016867684.1:p.Gly943Ala
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XM_017012196.1:c.2801G>C
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XP_016867685.1:p.Gly934Ala
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NM_000238.4:c.2978G>C
MANE Select
|
NP_000229.1:p.Gly993Ala
|
|
NM_172057.3:c.1958G>C
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NP_742054.1:p.Gly653Ala
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