ENST00000682114.1:c.572+53G>T
|
ENSP00000507245.1:n.572+53G>T
|
|
ENST00000682478.1:n.762+53G>T
|
|
|
ENST00000683576.1:n.815G>T
|
|
|
ENST00000683627.1:c.625G>T
|
ENSP00000507533.1:p.Glu209Ter
|
|
ENST00000684082.1:c.582G>T
|
ENSP00000508266.1:n.582G>T
|
|
ENST00000684633.1:n.597G>T
|
|
|
ENST00000684678.1:c.568+53G>T
|
ENSP00000507059.1:n.568+53G>T
|
|
ENST00000369842.9:c.625G>T
MANE Select
|
ENSP00000358857.4:p.Glu209Ter
|
|
ENST00000369835.3:c.520G>T
|
ENSP00000358850.3:p.Glu174Ter
|
|
ENST00000369842.8:c.625G>T
|
ENSP00000358857.4:p.Glu209Ter
|
|
ENST00000428228.5:c.*530G>T
|
ENSP00000401081.1:n.*530G>T
|
|
ENST00000471965.1:n.414G>T
|
|
|
ENST00000486738.5:n.1062G>T
|
|
|
ENST00000492448.1:n.608G>T
|
|
|
NM_000117.2:c.625G>T , LRG_745t1:c.625G>T
|
NP_000108.1:p.Glu209Ter
|
|
XM_024452349.1:c.631G>T
|
XP_024308117.1:p.Glu211Ter
|
|
NM_000117.3:c.625G>T
MANE Select
|
NP_000108.1:p.Glu209Ter
|
|