ENST00000486779.2:n.553A>T
|
|
|
ENST00000696333.1:c.1761A>T
|
ENSP00000512566.1:p.Thr587=
|
|
ENST00000696441.1:c.1761A>T
|
ENSP00000512631.1:p.Thr587=
|
|
ENST00000706664.1:n.1875A>T
|
|
|
ENST00000706666.1:n.1837A>T
|
|
|
ENST00000706667.1:n.2651A>T
|
|
|
ENST00000706668.1:n.2489A>T
|
|
|
ENST00000313164.10:c.1761A>T
MANE Select
|
ENSP00000322061.9:p.Thr587=
|
|
ENST00000313164.9:c.1761A>T
|
ENSP00000322061.9:p.Thr587=
|
|
ENST00000486779.1:n.274A>T
|
|
|
NM_000587.2:c.1761A>T , LRG_30t1:c.1761A>T
|
NP_000578.2:p.Thr587=
|
|
XM_011514122.1:c.1761A>T
|
XP_011512424.1:p.Thr587=
|
|
NM_000587.3:c.1761A>T
|
NP_000578.2:p.Thr587=
|
|
NM_000587.4:c.1761A>T
MANE Select
|
NP_000578.2:p.Thr587=
|
|