ENST00000261937.11:c.3895T>G
MANE Select
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ENSP00000261937.6:p.Cys1299Gly
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ENST00000261937.10:c.3895T>G
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ENSP00000261937.6:p.Cys1299Gly
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ENST00000502603.5:n.595T>G
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NM_182925.4:c.3895T>G
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NP_891555.2:p.Cys1299Gly
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XM_011534477.1:c.4144T>G
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XP_011532779.1:p.Cys1382Gly
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XM_011534478.1:c.4126T>G
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XP_011532780.1:p.Cys1376Gly
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XM_011534479.1:c.*41T>G
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XP_011532781.1:n.*41T>G
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XM_011534482.1:c.3913T>G
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XP_011532784.1:p.Cys1305Gly
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XM_011534483.1:c.3835T>G
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XP_011532785.1:p.Cys1279Gly
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XM_011534484.1:c.3436T>G
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XP_011532786.1:p.Cys1146Gly
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XR_941095.1:n.4181T>G
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XM_011534478.3:c.4126T>G
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XP_011532780.1:p.Cys1376Gly
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XM_011534484.2:c.3436T>G
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XP_011532786.1:p.Cys1146Gly
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XM_017009263.1:c.*41T>G
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XP_016864752.1:n.*41T>G
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XM_017009268.1:c.3817T>G
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XP_016864757.1:p.Cys1273Gly
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XR_001742050.2:n.4385T>G
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|
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NM_182925.5:c.3895T>G
MANE Select
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NP_891555.2:p.Cys1299Gly
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