ENST00000261819.8:c.1744A>C
MANE Select
|
ENSP00000261819.3:p.Ser582Arg
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ENST00000261819.7:c.1744A>C
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ENSP00000261819.3:p.Ser582Arg
|
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ENST00000441917.6:c.1408A>C
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ENSP00000415061.2:p.Ser470Arg
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ENST00000534976.5:n.2400A>C
|
|
|
ENST00000535482.1:c.742A>C
|
ENSP00000438754.1:p.Ser248Arg
|
|
ENST00000535641.5:n.1955A>C
|
|
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ENST00000539079.5:c.1088A>C
|
|
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ENST00000541887.5:c.1705A>C
|
ENSP00000439875.1:p.Ser569Arg
|
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ENST00000544314.5:n.862A>C
|
|
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ENST00000545218.5:n.987A>C
|
|
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NM_001137559.1:c.1408A>C
|
NP_001131031.1:p.Ser470Arg
|
|
NM_016237.4:c.1744A>C
|
NP_057321.2:p.Ser582Arg
|
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XM_005253900.2:c.1705A>C
|
XP_005253957.1:p.Ser569Arg
|
|
XM_006719449.1:c.550A>C
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XP_006719512.1:p.Ser184Arg
|
|
NM_001330489.1:c.1705A>C
|
NP_001317418.1:p.Ser569Arg
|
|
XM_017019423.2:c.550A>C
|
XP_016874912.1:p.Ser184Arg
|
|
XM_017019424.2:c.550A>C
|
XP_016874913.1:p.Ser184Arg
|
|
NM_016237.5:c.1744A>C
MANE Select
|
NP_057321.2:p.Ser582Arg
|
|
NM_001330489.2:c.1705A>C
|
NP_001317418.1:p.Ser569Arg
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