ENST00000264381.8:c.1799T>A
MANE Select
|
ENSP00000264381.3:p.Val600Glu
|
|
ENST00000264381.7:c.1799T>A
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ENSP00000264381.3:p.Val600Glu
|
|
ENST00000479451.5:c.389T>A
|
ENSP00000418325.1:p.Val130Glu
|
|
ENST00000482958.1:c.*305T>A
|
ENSP00000419804.1:n.*305T>A
|
|
ENST00000497011.5:c.*189T>A
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ENSP00000419505.1:n.*189T>A
|
|
NM_000055.2:c.1799T>A
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NP_000046.1:p.Val600Glu
|
|
XM_005247685.1:c.1922T>A
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XP_005247742.1:p.Val641Glu
|
|
NM_000055.3:c.1799T>A
|
NP_000046.1:p.Val600Glu
|
|
NR_137635.1:n.441T>A
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|
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NR_137636.1:n.2045T>A
|
|
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NM_000055.4:c.1799T>A
MANE Select
|
NP_000046.1:p.Val600Glu
|
|
NR_137635.2:n.392T>A
|
|
|
NR_137636.2:n.1996T>A
|
|
|