ENST00000326003.7:c.*330T>C
MANE Select
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ENSP00000314151.1:n.*330T>C
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ENST00000326003.6:c.*330T>C
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ENSP00000314151.1:n.*330T>C
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|
ENST00000360617.7:c.1558T>C
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ENSP00000353829.2:n.1558T>C
|
|
ENST00000422986.6:c.*772T>C
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ENSP00000393628.2:n.*772T>C
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|
ENST00000596333.1:n.1294T>C
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|
|
ENST00000601349.5:n.2395T>C
|
|
|
ENST00000617027.4:c.*330T>C
|
ENSP00000483513.1:n.*330T>C
|
|
NM_001030047.1:c.*841T>C
|
NP_001025218.1:n.*841T>C
|
|
NM_001030048.1:c.*330T>C
|
NP_001025219.1:n.*330T>C
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|
NM_001648.2:c.*330T>C
MANE Select
|
NP_001639.1:n.*330T>C
|
|
XM_011526923.1:c.*330T>C
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XP_011525225.1:n.*330T>C
|
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XR_935817.1:n.1324+1203T>C
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|
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