ENST00000563588.6:c.562T>C
MANE Select
|
ENSP00000455607.1:p.Cys188Arg
|
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ENST00000328273.11:c.562T>C
|
ENSP00000329968.7:p.Cys188Arg
|
|
ENST00000424889.7:c.562T>C
|
ENSP00000388571.3:p.Cys188Arg
|
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ENST00000563588.5:c.562T>C
|
ENSP00000455607.1:p.Cys188Arg
|
|
ENST00000563913.5:n.895T>C
|
|
|
ENST00000564838.5:n.931-403T>C
|
|
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ENST00000565897.5:c.562T>C
|
ENSP00000457359.1:p.Cys188Arg
|
|
ENST00000565924.5:c.562T>C
|
ENSP00000455091.1:p.Cys188Arg
|
|
ENST00000569684.1:n.974T>C
|
|
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NM_000294.2:c.562T>C
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NP_000285.1:p.Cys188Arg
|
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NM_001172432.1:c.562T>C
|
NP_001165903.1:p.Cys188Arg
|
|
NM_000294.3:c.562T>C
MANE Select
|
NP_000285.1:p.Cys188Arg
|
|
NM_001172432.2:c.562T>C
|
NP_001165903.1:p.Cys188Arg
|
|