ENST00000304611.13:c.1306C>A
MANE Select
|
ENSP00000303511.8:p.Pro436Thr
|
|
ENST00000244546.4:c.1306C>A
|
ENSP00000244546.4:p.Pro436Thr
|
|
ENST00000304611.12:c.1306C>A
|
ENSP00000303511.8:p.Pro436Thr
|
|
NM_000287.3:c.1306C>A
|
NP_000278.3:p.Pro436Thr
|
|
NM_001316313.1:c.1042C>A
|
NP_001303242.1:p.Pro348Thr
|
|
NR_133009.1:n.1399C>A
|
|
|
XM_011514661.1:c.1222C>A
|
XP_011512963.1:p.Pro408Thr
|
|
XR_926246.1:n.1399C>A
|
|
|
XM_011514661.2:c.1222C>A
|
XP_011512963.1:p.Pro408Thr
|
|
XR_001743466.2:n.2380C>A
|
|
|
NM_000287.4:c.1306C>A
MANE Select
|
NP_000278.3:p.Pro436Thr
|
|
NM_001316313.2:c.1042C>A
|
NP_001303242.1:p.Pro348Thr
|
|
NR_133009.2:n.1337C>A
|
|
|