|
NM_000287.4:c.759T>C
MANE Select
|
NP_000278.3:p.Asp253=
|
|
ENST00000304611.13:c.759T>C
MANE Select
|
ENSP00000303511.8:p.Asp253=
|
|
NM_000287.3:c.759T>C
|
NP_000278.3:p.Asp253=
|
|
NM_001316313.1:c.618+141T>C
|
NP_001303242.1:n.618+141T>C
|
|
NM_001316313.2:c.618+141T>C
|
NP_001303242.1:n.618+141T>C
|
|
NR_133009.1:n.852T>C
|
|
|
NR_133009.2:n.790T>C
|
|
|
ENST00000244546.4:c.759T>C
|
ENSP00000244546.4:p.Asp253=
|
|
ENST00000304611.12:c.759T>C
|
ENSP00000303511.8:p.Asp253=
|
|
XM_011514661.1:c.759T>C
|
XP_011512963.1:p.Asp253=
|
|
XM_011514661.2:c.759T>C
|
XP_011512963.1:p.Asp253=
|
|
XR_001743466.2:n.1833T>C
|
|
|
XR_926246.1:n.852T>C
|
|