ENST00000382103.7:c.387T>G
MANE Select
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ENSP00000371535.2:p.Ala129=
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ENST00000680581.1:c.387T>G
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ENSP00000506483.1:p.Ala129=
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ENST00000680824.1:n.1603T>G
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ENST00000681071.1:n.679T>G
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ENST00000681166.1:n.1434T>G
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ENST00000681341.1:n.1528T>G
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ENST00000681640.1:n.481T>G
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ENST00000681948.1:c.642T>G
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ENSP00000505991.1:p.Ala214=
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ENST00000358971.7:c.*185T>G
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ENSP00000351857.3:n.*185T>G
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ENST00000382103.6:c.387T>G
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ENSP00000371535.2:p.Ala129=
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ENST00000514585.5:c.*88T>G
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ENSP00000421880.1:n.*88T>G
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NM_016955.3:c.387T>G
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NP_058651.3:p.Ala129=
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XM_005248168.2:c.150T>G
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XP_005248225.1:p.Ala50=
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XM_006713965.2:c.207T>G
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XP_006714028.1:p.Ala69=
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XM_011513846.1:c.384T>G
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XP_011512148.1:p.Ala128=
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XM_011513847.1:c.354T>G
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XP_011512149.1:p.Ala118=
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XM_011513848.1:c.207T>G
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XP_011512150.1:p.Ala69=
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XM_011513846.2:c.384T>G
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XP_011512148.1:p.Ala128=
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XM_011513847.2:c.354T>G
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XP_011512149.1:p.Ala118=
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XM_017008277.1:c.642T>G
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XP_016863766.1:p.Ala214=
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XM_017008278.1:c.-37T>G
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XP_016863767.1:n.-37T>G
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NM_016955.4:c.387T>G
MANE Select
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NP_058651.3:p.Ala129=
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