ENST00000344922.10:c.4663G>T
MANE Select
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ENSP00000340900.5:p.Ala1555Ser
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ENST00000340535.11:c.1297G>T
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ENSP00000345866.7:p.Ala433Ser
|
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ENST00000344507.1:c.1475-6822G>T
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ENSP00000341348.1:n.1475-6822G>T
|
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ENST00000344922.9:c.4663G>T
|
ENSP00000340900.5:p.Ala1555Ser
|
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ENST00000476400.1:n.136G>T
|
|
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NM_001300867.1:c.1297G>T
|
NP_001287796.1:p.Ala433Ser
|
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NM_198551.3:c.4663G>T
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NP_940953.2:p.Ala1555Ser
|
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XM_005273121.3:c.4663G>T
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XP_005273178.1:p.Ala1555Ser
|
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XM_006711304.2:c.4486G>T
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XP_006711367.1:p.Ala1496Ser
|
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NM_001324062.1:c.4663G>T
|
NP_001310991.1:p.Ala1555Ser
|
|
NM_001324063.1:c.4486G>T
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NP_001310992.1:p.Ala1496Ser
|
|
NM_001324064.1:c.4171G>T
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NP_001310993.1:p.Ala1391Ser
|
|
NM_001324065.1:c.1297G>T
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NP_001310994.1:p.Ala433Ser
|
|
XM_006711304.4:c.4486G>T
|
XP_006711367.3:p.Ala1496Ser
|
|
XM_017001243.2:c.4171G>T
|
XP_016856732.1:p.Ala1391Ser
|
|
NM_198551.4:c.4663G>T
MANE Select
|
NP_940953.2:p.Ala1555Ser
|
|
NM_001300867.2:c.1297G>T
|
NP_001287796.1:p.Ala433Ser
|
|
NM_001324062.2:c.4663G>T
|
NP_001310991.1:p.Ala1555Ser
|
|
NM_001324063.2:c.4486G>T
|
NP_001310992.1:p.Ala1496Ser
|
|
NM_001324064.2:c.4171G>T
|
NP_001310993.1:p.Ala1391Ser
|
|
NM_001324065.2:c.1297G>T
|
NP_001310994.1:p.Ala433Ser
|
|