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NM_001080414.4:c.5209G>A
MANE Select
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NP_001073883.2:p.Ala1737Thr
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ENST00000389857.11:c.5209G>A
MANE Select
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ENSP00000374507.6:p.Ala1737Thr
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NM_001080414.3:c.5209G>A
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NP_001073883.2:p.Ala1737Thr
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ENST00000331194.8:c.781G>A
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ENSP00000330332.8:p.Ala261Thr
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ENST00000334448.5:n.1021G>A
|
|
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ENST00000389857.10:c.5209G>A
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ENSP00000374507.6:p.Ala1737Thr
|
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ENST00000556726.5:c.1437G>A
|
|
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XM_011536796.1:c.5101G>A
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XP_011535098.1:p.Ala1701Thr
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XM_011536796.2:c.5101G>A
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XP_011535098.1:p.Ala1701Thr
|
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XM_017021336.1:c.2290G>A
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XP_016876825.1:p.Ala764Thr
|
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XR_429316.2:n.5484G>A
|
|
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XR_429316.4:n.5482G>A
|
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