ENST00000262493.12:c.779T>G
MANE Select
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ENSP00000262493.6:p.Phe260Cys
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ENST00000562316.6:c.446T>G
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ENSP00000457238.2:p.Phe149Cys
|
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ENST00000564727.2:c.83T>G
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ENSP00000454971.2:p.Phe28Cys
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ENST00000568375.2:c.116-3427T>G
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|
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ENST00000638185.1:n.994T>G
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|
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ENST00000638210.1:n.1079T>G
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|
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ENST00000638705.1:c.779T>G
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ENSP00000491223.1:p.Phe260Cys
|
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ENST00000638836.1:n.689T>G
|
|
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ENST00000639055.1:n.1500T>G
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ENST00000639251.1:n.680T>G
|
|
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ENST00000639268.1:c.414T>G
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ENST00000639341.1:c.304T>G
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|
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ENST00000639770.1:c.817T>G
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ENSP00000491999.1:n.817T>G
|
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ENST00000640390.1:n.709T>G
|
|
|
ENST00000640469.1:c.143T>G
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ENSP00000491875.1:p.Phe48Cys
|
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ENST00000640560.1:n.555T>G
|
|
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ENST00000640893.1:c.*177T>G
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ENSP00000492677.1:n.*177T>G
|
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ENST00000262493.10:c.779T>G
|
ENSP00000262493.6:p.Phe260Cys
|
|
ENST00000568375.1:n.116-3427T>G
|
|
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NM_020988.2:c.779T>G
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NP_066268.1:p.Phe260Cys
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XM_011523003.1:c.653T>G
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XP_011521305.1:p.Phe218Cys
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XM_011523003.3:c.653T>G
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XP_011521305.1:p.Phe218Cys
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NM_020988.3:c.779T>G
MANE Select
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NP_066268.1:p.Phe260Cys
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