ENST00000326003.7:c.778A>C
MANE Select
|
ENSP00000314151.1:p.Asn260His
|
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ENST00000326003.6:c.778A>C
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ENSP00000314151.1:p.Asn260His
|
|
ENST00000360617.7:c.1220A>C
|
ENSP00000353829.2:n.1220A>C
|
|
ENST00000422986.6:c.*434A>C
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ENSP00000393628.2:n.*434A>C
|
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ENST00000595392.5:c.*279A>C
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ENSP00000468912.1:n.*279A>C
|
|
ENST00000595952.5:c.649A>C
|
ENSP00000471155.1:p.Asn217His
|
|
ENST00000596333.1:n.956A>C
|
|
|
ENST00000598145.1:c.780A>C
|
|
|
ENST00000601349.5:n.2057A>C
|
|
|
ENST00000601812.1:n.1210A>C
|
|
|
ENST00000617027.4:c.655A>C
|
ENSP00000483513.1:p.Asn219His
|
|
NM_001030047.1:c.*503A>C
|
NP_001025218.1:n.*503A>C
|
|
NM_001030048.1:c.649A>C
|
NP_001025219.1:p.Asn217His
|
|
NM_001648.2:c.778A>C
MANE Select
|
NP_001639.1:p.Asn260His
|
|
XM_011526923.1:c.796A>C
|
XP_011525225.1:p.Asn266His
|
|
XR_935817.1:n.1324+865A>C
|
|
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