ENST00000461280.2:n.656C>A
|
|
|
ENST00000684116.1:n.251C>A
|
|
|
ENST00000684241.1:n.2191C>A
|
|
|
ENST00000262186.10:c.1358C>A
MANE Select
|
ENSP00000262186.5:p.Ala453Asp
|
|
ENST00000330883.9:c.338C>A
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ENSP00000328531.4:p.Ala113Asp
|
|
ENST00000262186.9:c.1358C>A
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ENSP00000262186.5:p.Ala453Asp
|
|
ENST00000330883.8:c.338C>A
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ENSP00000328531.4:p.Ala113Asp
|
|
ENST00000430723.4:c.1010C>A
|
ENSP00000387657.4:p.Ala337Asp
|
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ENST00000461280.1:n.645C>A
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|
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ENST00000473610.5:n.663C>A
|
|
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ENST00000532957.5:n.1581C>A
|
|
|
NM_000238.3:c.1358C>A , LRG_288t1:c.1358C>A
|
NP_000229.1:p.Ala453Asp
|
|
NM_001204798.1:c.338C>A
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NP_001191727.1:p.Ala113Asp
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|
NM_172056.2:c.1358C>A , LRG_288t2:c.1358C>A
|
NP_742053.1:p.Ala453Asp
|
|
NM_172057.2:c.338C>A , LRG_288t3:c.338C>A
|
NP_742054.1:p.Ala113Asp
|
|
XM_011516185.1:c.1058C>A
|
XP_011514487.1:p.Ala353Asp
|
|
XM_011516186.1:c.1358C>A
|
XP_011514488.1:p.Ala453Asp
|
|
XM_011516185.2:c.1058C>A
|
XP_011514487.1:p.Ala353Asp
|
|
XM_011516186.3:c.1358C>A
|
XP_011514488.1:p.Ala453Asp
|
|
XM_017012195.1:c.1208C>A
|
XP_016867684.1:p.Ala403Asp
|
|
XM_017012196.1:c.1181C>A
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XP_016867685.1:p.Ala394Asp
|
|
NM_000238.4:c.1358C>A
MANE Select
|
NP_000229.1:p.Ala453Asp
|
|
NM_001204798.2:c.338C>A
|
NP_001191727.1:p.Ala113Asp
|
|
NM_172057.3:c.338C>A
|
NP_742054.1:p.Ala113Asp
|
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