ENST00000355832.10:c.3634T>C
MANE Select
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ENSP00000348089.5:p.Cys1212Arg
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ENST00000679552.1:n.705T>C
|
|
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ENST00000679871.1:n.780T>C
|
|
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ENST00000679974.1:n.683T>C
|
|
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ENST00000681632.1:n.5037T>C
|
|
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ENST00000681659.1:c.3475T>C
|
ENSP00000505631.1:p.Cys1159Arg
|
|
ENST00000355832.9:c.3634T>C
|
ENSP00000348089.5:p.Cys1212Arg
|
|
ENST00000623073.3:c.*1930T>C
|
ENSP00000485650.1:n.*1930T>C
|
|
ENST00000623115.3:c.1744T>C
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ENSP00000485321.1:p.Cys582Arg
|
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ENST00000624341.3:c.1466T>C
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|
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NM_000124.3:c.3634T>C
|
NP_000115.1:p.Cys1212Arg
|
|
XR_945953.1:n.243-1239A>G
|
|
|
NM_001346440.1:c.3634T>C
|
NP_001333369.1:p.Cys1212Arg
|
|
NM_000124.4:c.3634T>C
MANE Select
|
NP_000115.1:p.Cys1212Arg
|
|
NM_001346440.2:c.3634T>C
|
NP_001333369.1:p.Cys1212Arg
|
|