ENST00000233575.7:c.817C>T
MANE Select
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ENSP00000233575.2:p.Arg273Cys
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ENST00000233575.6:c.817C>T
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ENSP00000233575.2:p.Arg273Cys
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ENST00000427123.5:c.*627C>T
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ENSP00000405399.1:n.*627C>T
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ENST00000440760.5:c.*662C>T
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ENSP00000399727.1:n.*662C>T
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ENST00000453453.1:c.*344C>T
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ENSP00000401922.1:n.*344C>T
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ENST00000493711.1:n.534C>T
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|
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ENST00000537606.5:c.742C>T
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ENSP00000439208.1:p.Arg248Cys
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NM_001267059.1:c.781C>T
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NP_001253988.1:p.Arg261Cys
|
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NM_001267060.1:c.742C>T
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NP_001253989.1:p.Arg248Cys
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NM_001267061.1:c.757C>T
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NP_001253990.1:p.Arg253Cys
|
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NM_014748.3:c.817C>T
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NP_055563.1:p.Arg273Cys
|
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NR_049782.1:n.1190C>T
|
|
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NR_049783.1:n.1163C>T
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|
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NR_049784.1:n.1139C>T
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|
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NR_049785.1:n.1072C>T
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|
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NR_049786.1:n.1021C>T
|
|
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NR_049787.1:n.872C>T
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|
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NR_049788.1:n.802C>T
|
|
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XM_011533203.1:c.175C>T
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XP_011531505.1:p.Arg59Cys
|
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XM_011533203.2:c.175C>T
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XP_011531505.1:p.Arg59Cys
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XM_017005405.2:c.175C>T
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XP_016860894.1:p.Arg59Cys
|
|
NM_014748.4:c.817C>T
MANE Select
|
NP_055563.1:p.Arg273Cys
|
|
NM_001267059.2:c.781C>T
|
NP_001253988.1:p.Arg261Cys
|
|
NM_001267061.2:c.757C>T
|
NP_001253990.1:p.Arg253Cys
|
|
NR_049782.2:n.1070C>T
|
|
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NR_049783.2:n.1043C>T
|
|
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NR_049784.2:n.1019C>T
|
|
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NR_049785.2:n.952C>T
|
|
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NR_049786.2:n.901C>T
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|
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NR_049787.2:n.752C>T
|
|
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NR_049788.2:n.682C>T
|
|
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NM_001267060.2:c.742C>T
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NP_001253989.1:p.Arg248Cys
|
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