|
NM_002049.4:c.871-7T>C
MANE Select
|
NP_002040.1:n.871-7T>C
|
|
ENST00000376670.9:c.871-7T>C
MANE Select
|
ENSP00000365858.3:n.871-7T>C
|
|
NM_002049.3:c.871-7T>C , LRG_559t1:c.871-7T>C
|
NP_002040.1:n.871-7T>C
|
|
ENST00000376665.4:c.871-348T>C
|
ENSP00000365853.3:n.871-348T>C
|
|
ENST00000376670.7:c.871-7T>C
|
ENSP00000365858.3:n.871-7T>C
|
|
ENST00000651144.1:c.622-7T>C
|
ENSP00000498550.1:n.622-7T>C
|
|
ENST00000651144.2:c.622-7T>C
|
ENSP00000498550.1:n.622-7T>C
|
|
ENST00000696450.1:c.879T>C
|
ENSP00000512637.1:p.Phe293=
|
|
ENST00000696451.1:c.630T>C
|
ENSP00000512638.1:p.Phe210=
|
|
ENST00000696452.1:c.654T>C
|
ENSP00000512639.1:p.Phe218=
|
|
XM_011543897.1:c.879T>C
|
XP_011542199.1:p.Phe293=
|
|
XM_011543897.2:c.879T>C
|
XP_011542199.1:p.Phe293=
|
|
XM_011543898.1:c.630T>C
|
XP_011542200.1:p.Phe210=
|
|
XM_011543898.2:c.630T>C
|
XP_011542200.1:p.Phe210=
|
|
XM_024452363.1:c.622-7T>C
|
XP_024308131.1:n.622-7T>C
|