ENST00000682275.1:c.2395G>A
|
ENSP00000507852.1:p.Ala799Thr
|
|
ENST00000683395.1:c.2336G>A
|
|
|
ENST00000684087.1:c.2359G>A
|
ENSP00000506978.1:p.Ala787Thr
|
|
ENST00000506362.2:c.2110G>A
|
ENSP00000424103.2:p.Ala704Thr
|
|
ENST00000673991.1:c.2395G>A
|
ENSP00000501033.1:p.Ala799Thr
|
|
ENST00000226760.5:c.2359G>A
MANE Select
|
ENSP00000226760.1:p.Ala787Thr
|
|
ENST00000503569.5:c.2359G>A
|
ENSP00000423337.1:p.Ala787Thr
|
|
ENST00000507765.1:n.2544G>A
|
|
|
NM_001145853.1:c.2359G>A
|
NP_001139325.1:p.Ala787Thr
|
|
NM_006005.3:c.2359G>A
MANE Select
|
NP_005996.2:p.Ala787Thr
|
|
XM_017008586.1:c.2368G>A
|
XP_016864075.1:p.Ala790Thr
|
|