ENST00000355832.10:c.3939C>A
MANE Select
|
ENSP00000348089.5:p.Thr1313=
|
|
ENST00000679552.1:n.1010C>A
|
|
|
ENST00000679871.1:n.1085C>A
|
|
|
ENST00000679974.1:n.988C>A
|
|
|
ENST00000681632.1:n.5342C>A
|
|
|
ENST00000681659.1:c.3780C>A
|
ENSP00000505631.1:p.Thr1260=
|
|
ENST00000355832.9:c.3939C>A
|
ENSP00000348089.5:p.Thr1313=
|
|
ENST00000465653.1:n.261C>A
|
|
|
ENST00000623073.3:c.*2235C>A
|
ENSP00000485650.1:n.*2235C>A
|
|
ENST00000623115.3:c.2049C>A
|
ENSP00000485321.1:p.Thr683=
|
|
ENST00000624341.3:c.1771C>A
|
|
|
NM_000124.3:c.3939C>A
|
NP_000115.1:p.Thr1313=
|
|
XR_945953.1:n.243-10169G>T
|
|
|
NM_001346440.1:c.3939C>A
|
NP_001333369.1:p.Thr1313=
|
|
NM_000124.4:c.3939C>A
MANE Select
|
NP_000115.1:p.Thr1313=
|
|
NM_001346440.2:c.3939C>A
|
NP_001333369.1:p.Thr1313=
|
|