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NM_018052.5:c.1744G>T
MANE Select
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NP_060522.3:p.Ala582Ser
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ENST00000261776.10:c.1744G>T
MANE Select
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ENSP00000261776.5:p.Ala582Ser
|
|
NM_001351157.1:c.1042G>T
|
NP_001338086.1:p.Ala348Ser
|
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NM_001351157.2:c.1042G>T
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NP_001338086.1:p.Ala348Ser
|
|
NM_018052.3:c.1744G>T
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NP_060522.3:p.Ala582Ser
|
|
NM_018052.4:c.1744G>T
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NP_060522.3:p.Ala582Ser
|
|
ENST00000261776.9:c.1744G>T
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ENSP00000261776.5:p.Ala582Ser
|
|
ENST00000536184.6:c.40G>T
|
ENSP00000439284.2:p.Ala14Ser
|
|
ENST00000564685.5:n.432G>T
|
|
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ENST00000566416.1:c.374G>T
|
|
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ENST00000568548.5:c.*1470G>T
|
ENSP00000454650.1:n.*1470G>T
|
|
ENST00000568886.5:c.*369G>T
|
ENSP00000457809.1:n.*369G>T
|
|
XM_005256038.2:c.1744G>T
|
XP_005256095.1:p.Ala582Ser
|
|
XM_005256038.4:c.1744G>T
|
XP_005256095.1:p.Ala582Ser
|