NM_015144.3:c.2350G>A
MANE Select
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NP_055959.2:p.Ala784Thr
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ENST00000671377.2:c.2350G>A
MANE Select
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ENSP00000499622.1:p.Ala784Thr
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NM_015144.2:c.1939G>A
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NP_055959.1:p.Ala647Thr
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ENST00000268616.8:c.1939G>A
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ENSP00000268616.4:p.Ala647Thr
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ENST00000268616.9:c.1939G>A
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ENSP00000268616.4:p.Ala647Thr
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ENST00000561928.1:c.1589G>A
|
|
ENST00000568020.5:c.1939G>A
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ENSP00000455431.1:p.Ala647Thr
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ENST00000568020.6:c.1971G>A
|
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XM_005255858.3:c.1939G>A
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XP_005255915.2:p.Ala647Thr
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XM_017023082.2:c.1831G>A
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XP_016878571.1:p.Ala611Thr
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XR_243401.3:n.2157G>A
|
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