ENST00000326003.7:c.*37A>C
MANE Select
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ENSP00000314151.1:n.*37A>C
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ENST00000326003.6:c.*37A>C
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ENSP00000314151.1:n.*37A>C
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|
ENST00000360617.7:c.1265A>C
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ENSP00000353829.2:n.1265A>C
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ENST00000422986.6:c.*479A>C
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ENSP00000393628.2:n.*479A>C
|
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ENST00000595392.5:c.*324A>C
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ENSP00000468912.1:n.*324A>C
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|
ENST00000595952.5:c.*37A>C
|
ENSP00000471155.1:n.*37A>C
|
|
ENST00000596333.1:n.1001A>C
|
|
|
ENST00000598145.1:c.825A>C
|
|
|
ENST00000601349.5:n.2102A>C
|
|
|
ENST00000617027.4:c.*37A>C
|
ENSP00000483513.1:n.*37A>C
|
|
NM_001030047.1:c.*548A>C
|
NP_001025218.1:n.*548A>C
|
|
NM_001030048.1:c.*37A>C
|
NP_001025219.1:n.*37A>C
|
|
NM_001648.2:c.*37A>C
MANE Select
|
NP_001639.1:n.*37A>C
|
|
XM_011526923.1:c.*37A>C
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XP_011525225.1:n.*37A>C
|
|
XR_935817.1:n.1324+910A>C
|
|
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