ENST00000264381.8:c.1795T>A
MANE Select
|
ENSP00000264381.3:p.Cys599Ser
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|
ENST00000264381.7:c.1795T>A
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ENSP00000264381.3:p.Cys599Ser
|
|
ENST00000479451.5:c.385T>A
|
ENSP00000418325.1:p.Cys129Ser
|
|
ENST00000482958.1:c.*301T>A
|
ENSP00000419804.1:n.*301T>A
|
|
ENST00000497011.5:c.*185T>A
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ENSP00000419505.1:n.*185T>A
|
|
NM_000055.2:c.1795T>A
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NP_000046.1:p.Cys599Ser
|
|
XM_005247685.1:c.1918T>A
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XP_005247742.1:p.Cys640Ser
|
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NM_000055.3:c.1795T>A
|
NP_000046.1:p.Cys599Ser
|
|
NR_137635.1:n.437T>A
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|
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NR_137636.1:n.2041T>A
|
|
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NM_000055.4:c.1795T>A
MANE Select
|
NP_000046.1:p.Cys599Ser
|
|
NR_137635.2:n.388T>A
|
|
|
NR_137636.2:n.1992T>A
|
|
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