|
NM_006767.4:c.320G>C
MANE Select
|
NP_006758.2:p.Arg107Thr
|
|
ENST00000646124.2:c.320G>C
MANE Select
|
ENSP00000496779.1:p.Arg107Thr
|
|
NM_006767.3:c.320G>C
|
NP_006758.2:p.Arg107Thr
|
|
ENST00000215739.12:c.320G>C
|
ENSP00000215739.8:p.Arg107Thr
|
|
ENST00000414985.5:c.320G>C
|
ENSP00000397247.1:p.Arg107Thr
|
|
ENST00000443265.5:c.*19G>C
|
ENSP00000406466.1:n.*19G>C
|
|
ENST00000479606.5:n.466G>C
|
|
|
ENST00000493460.1:n.395G>C
|
|
|
ENST00000493460.2:n.395G>C
|
|
|
ENST00000642151.1:c.231G>C
|
|
|
ENST00000644435.1:c.226G>C
|
|
|
ENST00000645935.1:c.264-1607G>C
|
ENSP00000493479.1:n.264-1607G>C
|
|
ENST00000700578.1:c.320G>C
|
ENSP00000515073.1:p.Arg107Thr
|