ENST00000333371.8:c.1399G>T
MANE Select
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ENSP00000327650.4:p.Ala467Ser
|
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ENST00000643536.1:c.1399G>T
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ENSP00000494429.1:p.Ala467Ser
|
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ENST00000647331.1:c.1399G>T
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ENSP00000493953.1:p.Ala467Ser
|
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ENST00000333371.7:c.1399G>T
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ENSP00000327650.3:p.Ala467Ser
|
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ENST00000535906.1:c.1318G>T
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ENSP00000444053.1:p.Ala440Ser
|
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ENST00000574755.5:c.*1094G>T
|
ENSP00000460413.1:n.*1094G>T
|
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NM_001289148.1:c.1318G>T
|
NP_001276077.1:p.Ala440Ser
|
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NM_001289149.1:c.1126G>T
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NP_001276078.1:p.Ala376Ser
|
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NM_018668.4:c.1399G>T , LRG_884t1:c.1399G>T
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NP_061138.3:p.Ala467Ser
|
|
XM_005254884.2:c.1321G>T
|
XP_005254941.1:p.Ala441Ser
|
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XM_005254887.1:c.1126G>T
|
XP_005254944.1:p.Ala376Ser
|
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XM_011521448.1:c.1126G>T
|
XP_011519750.1:p.Ala376Ser
|
|
XM_011521449.1:c.1075G>T
|
XP_011519751.1:p.Ala359Ser
|
|
XM_011521449.2:c.1075G>T
|
XP_011519751.1:p.Ala359Ser
|
|
XM_017022075.2:c.1054G>T
|
XP_016877564.1:p.Ala352Ser
|
|
XM_017022076.1:c.1054G>T
|
XP_016877565.1:p.Ala352Ser
|
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XR_001751213.2:n.1897G>T
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|
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NM_018668.5:c.1399G>T
MANE Select
|
NP_061138.3:p.Ala467Ser
|
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