ENST00000684241.1:n.1678C>A
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|
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ENST00000262186.10:c.845C>A
MANE Select
|
ENSP00000262186.5:p.Ala282Asp
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|
ENST00000262186.9:c.845C>A
|
ENSP00000262186.5:p.Ala282Asp
|
|
ENST00000430723.4:c.497C>A
|
ENSP00000387657.4:p.Ala166Asp
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ENST00000532957.5:n.1068C>A
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NM_000238.3:c.845C>A , LRG_288t1:c.845C>A
|
NP_000229.1:p.Ala282Asp
|
|
NM_172056.2:c.845C>A , LRG_288t2:c.845C>A
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NP_742053.1:p.Ala282Asp
|
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XM_011516185.1:c.545C>A
|
XP_011514487.1:p.Ala182Asp
|
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XM_011516186.1:c.845C>A
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XP_011514488.1:p.Ala282Asp
|
|
XM_011516185.2:c.545C>A
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XP_011514487.1:p.Ala182Asp
|
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XM_011516186.3:c.845C>A
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XP_011514488.1:p.Ala282Asp
|
|
XM_017012195.1:c.695C>A
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XP_016867684.1:p.Ala232Asp
|
|
XM_017012196.1:c.668C>A
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XP_016867685.1:p.Ala223Asp
|
|
NM_000238.4:c.845C>A
MANE Select
|
NP_000229.1:p.Ala282Asp
|
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