ENST00000309424.8:c.147A>T
MANE Select
|
ENSP00000310966.3:p.Ala49=
|
|
ENST00000309424.7:c.147A>T
|
ENSP00000310966.3:p.Ala49=
|
|
ENST00000589804.1:c.153A>T
|
ENSP00000465099.1:p.Ala51=
|
|
ENST00000590794.1:c.20+500A>T
|
|
|
ENST00000592852.1:c.-388A>T
|
ENSP00000467771.1:n.-388A>T
|
|
NM_001297590.1:c.153A>T
|
NP_001284519.1:p.Ala51=
|
|
NM_012099.1:c.147A>T
|
NP_036231.1:p.Ala49=
|
|
NM_001297590.2:c.153A>T
|
NP_001284519.1:p.Ala51=
|
|
NM_012099.2:c.147A>T
|
NP_036231.1:p.Ala49=
|
|
NM_001297590.3:c.153A>T
|
NP_001284519.1:p.Ala51=
|
|
NM_012099.3:c.147A>T
MANE Select
|
NP_036231.1:p.Ala49=
|
|