ENST00000405460.9:c.11521A>G
MANE Select
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ENSP00000384582.2:p.Thr3841Ala
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ENST00000425867.3:c.652A>G
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ENSP00000392618.3:p.Thr218Ala
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ENST00000639431.1:c.265+78917A>G
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ENSP00000491057.1:n.265+78917A>G
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ENST00000640374.1:n.4665A>G
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ENST00000640464.1:n.1940A>G
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ENST00000405460.6:c.11521A>G
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ENSP00000384582.2:p.Thr3841Ala
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ENST00000509621.1:c.4218A>G
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NM_032119.3:c.11521A>G
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NP_115495.3:p.Thr3841Ala
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NR_003149.1:n.11534A>G
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XM_011543675.1:c.11518A>G
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XP_011541977.1:p.Thr3840Ala
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XM_011543676.1:c.11440A>G
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XP_011541978.1:p.Thr3814Ala
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XM_011543677.1:c.8824A>G
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XP_011541979.1:p.Thr2942Ala
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XM_011543678.1:c.11521A>G
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XP_011541980.1:p.Thr3841Ala
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NM_032119.4:c.11521A>G
MANE Select
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NP_115495.3:p.Thr3841Ala
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XM_017009963.2:c.11542A>G
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XP_016865452.1:p.Thr3848Ala
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XM_017009964.2:c.11539A>G
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XP_016865453.1:p.Thr3847Ala
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XM_017009965.1:c.11539A>G
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XP_016865454.1:p.Thr3847Ala
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XM_017009966.2:c.11461A>G
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XP_016865455.1:p.Thr3821Ala
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XM_017009967.1:c.11446A>G
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XP_016865456.1:p.Thr3816Ala
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XM_017009968.2:c.11542A>G
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XP_016865457.1:p.Thr3848Ala
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XM_017009969.2:c.11542A>G
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XP_016865458.1:p.Thr3848Ala
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XM_017009970.2:c.11542A>G
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XP_016865459.1:p.Thr3848Ala
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XM_017009971.2:c.11542A>G
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XP_016865460.1:p.Thr3848Ala
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XM_017009972.1:c.4660A>G
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XP_016865461.1:p.Thr1554Ala
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XM_017009973.1:c.4639A>G
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XP_016865462.1:p.Thr1547Ala
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NR_003149.2:n.11537A>G
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