ENST00000264690.11:c.427A>C
MANE Select
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ENSP00000264690.6:p.Ser143Arg
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|
ENST00000264690.10:c.427A>C
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ENSP00000264690.6:p.Ser143Arg
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|
ENST00000428196.5:c.427A>C
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ENSP00000412366.1:p.Ser143Arg
|
|
ENST00000446598.6:c.313A>C
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ENSP00000415563.2:p.Ser105Arg
|
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ENST00000511406.5:n.457A>C
|
|
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ENST00000511608.5:c.570A>C
|
|
|
ENST00000513864.2:c.313A>C
|
ENSP00000424469.2:p.Ser105Arg
|
|
NM_000892.3:c.427A>C
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NP_000883.2:p.Ser143Arg
|
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XM_011531930.1:c.427A>C
|
XP_011530232.1:p.Ser143Arg
|
|
XM_011531931.1:c.427A>C
|
XP_011530233.1:p.Ser143Arg
|
|
XM_011531932.1:c.313A>C
|
XP_011530234.1:p.Ser105Arg
|
|
XM_011531933.1:c.313A>C
|
XP_011530235.1:p.Ser105Arg
|
|
XM_011531934.1:c.-211A>C
|
XP_011530236.1:n.-211A>C
|
|
NM_000892.4:c.427A>C
|
NP_000883.2:p.Ser143Arg
|
|
NM_001318394.1:c.313A>C
|
NP_001305323.1:p.Ser105Arg
|
|
NM_001318396.1:c.-211A>C
|
NP_001305325.1:n.-211A>C
|
|
XM_011531930.2:c.427A>C
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XP_011530232.1:p.Ser143Arg
|
|
XM_017008181.1:c.427A>C
|
XP_016863670.1:p.Ser143Arg
|
|
XM_017008182.1:c.427A>C
|
XP_016863671.1:p.Ser143Arg
|
|
XM_017008183.1:c.427A>C
|
XP_016863672.1:p.Ser143Arg
|
|
NM_000892.5:c.427A>C
MANE Select
|
NP_000883.2:p.Ser143Arg
|
|
NM_001318394.2:c.313A>C
|
NP_001305323.1:p.Ser105Arg
|
|
NM_001318396.2:c.-211A>C
|
NP_001305325.1:n.-211A>C
|
|