|
NM_006767.4:c.200+1G>T
MANE Select
|
NP_006758.2:n.200+1G>T
|
|
ENST00000646124.2:c.200+1G>T
MANE Select
|
ENSP00000496779.1:n.200+1G>T
|
|
NM_006767.3:c.200+1G>T
|
NP_006758.2:n.200+1G>T
|
|
ENST00000215739.12:c.200+1G>T
|
ENSP00000215739.8:n.200+1G>T
|
|
ENST00000414985.5:c.200+1G>T
|
ENSP00000397247.1:n.200+1G>T
|
|
ENST00000443265.5:c.201G>T
|
ENSP00000406466.1:p.Arg67=
|
|
ENST00000479606.5:n.347-455G>T
|
|
|
ENST00000493460.1:n.275+1G>T
|
|
|
ENST00000493460.2:n.275+1G>T
|
|
|
ENST00000642151.1:c.78+1G>T
|
|
|
ENST00000644435.1:c.106+1G>T
|
|
|
ENST00000645935.1:c.200+1G>T
|
ENSP00000493479.1:n.200+1G>T
|
|
ENST00000700578.1:c.200+1G>T
|
ENSP00000515073.1:n.200+1G>T
|