ENST00000339077.10:c.1137T>A
MANE Select
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ENSP00000343273.4:p.Ala379=
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|
ENST00000339077.9:c.1137T>A
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ENSP00000343273.4:p.Ala379=
|
|
ENST00000409689.5:c.993T>A
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ENSP00000386263.1:p.Ala331=
|
|
ENST00000469576.1:n.24T>A
|
|
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ENST00000521082.5:c.*1145T>A
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ENSP00000430351.1:n.*1145T>A
|
|
NM_001031710.2:c.1137T>A
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NP_001026880.2:p.Ala379=
|
|
NM_018846.4:c.993T>A
|
NP_061334.4:p.Ala331=
|
|
NR_033328.1:n.1561T>A
|
|
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XM_006715753.1:c.1176T>A
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XP_006715816.1:p.Ala392=
|
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XM_006715754.1:c.1110T>A
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XP_006715817.1:p.Ala370=
|
|
XM_006715755.1:c.1110T>A
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XP_006715818.1:p.Ala370=
|
|
XM_006715756.1:c.1032T>A
|
XP_006715819.1:p.Ala344=
|
|
XM_006715753.3:c.1176T>A
|
XP_006715816.1:p.Ala392=
|
|
XM_006715754.3:c.1110T>A
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XP_006715817.1:p.Ala370=
|
|
XM_006715755.3:c.1110T>A
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XP_006715818.1:p.Ala370=
|
|
XM_006715756.3:c.1032T>A
|
XP_006715819.1:p.Ala344=
|
|
XM_017012439.2:c.1071T>A
|
XP_016867928.1:p.Ala357=
|
|
NM_001031710.3:c.1137T>A
MANE Select
|
NP_001026880.2:p.Ala379=
|
|
NM_018846.5:c.993T>A
|
NP_061334.4:p.Ala331=
|
|
NR_033328.2:n.1510T>A
|
|
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