ENST00000449291.7:c.1593T>A
MANE Select
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ENSP00000401508.2:p.Ser531Arg
|
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ENST00000340490.7:c.1678T>A
|
ENSP00000341136.3:p.Ser560Thr
|
|
ENST00000426292.7:c.1554T>A
|
ENSP00000390949.3:p.Ser518Arg
|
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ENST00000435154.7:c.*302T>A
|
ENSP00000405670.3:n.*302T>A
|
|
ENST00000449291.6:c.1593T>A
|
ENSP00000401508.2:p.Ser531Arg
|
|
ENST00000460623.5:c.617T>A
|
|
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ENST00000464332.5:n.1137T>A
|
|
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ENST00000498076.5:n.372T>A
|
|
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ENST00000529179.1:n.377T>A
|
|
|
NM_001286829.1:c.1554T>A
|
NP_001273758.1:p.Ser518Arg
|
|
NM_145201.5:c.1593T>A
|
NP_660202.3:p.Ser531Arg
|
|
XM_011517377.1:c.1330T>A
|
XP_011515679.1:p.Ser444Thr
|
|
NM_001363145.1:c.1512T>A
|
NP_001350074.1:p.Ser504Arg
|
|
NM_001363146.1:c.909T>A
|
NP_001350075.1:p.Ser303Arg
|
|
XM_017013975.2:c.1897T>A
|
XP_016869464.1:p.Ser633Thr
|
|
XM_017013976.2:c.1812T>A
|
XP_016869465.1:p.Ser604Arg
|
|
XM_017013977.2:c.1597T>A
|
XP_016869466.1:p.Ser533Thr
|
|
XM_017013978.2:c.1549T>A
|
XP_016869467.1:p.Ser517Thr
|
|
XM_017013979.2:c.994T>A
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XP_016869468.1:p.Ser332Thr
|
|
XM_024447332.1:c.967T>A
|
XP_024303100.1:p.Ser323Thr
|
|
XM_024447333.1:c.913T>A
|
XP_024303101.1:p.Ser305Thr
|
|
NM_145201.6:c.1593T>A
MANE Select
|
NP_660202.3:p.Ser531Arg
|
|
NM_001286829.2:c.1554T>A
|
NP_001273758.1:p.Ser518Arg
|
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