ENST00000578493.2:n.749G>T
|
|
|
ENST00000699291.1:c.541G>T
|
ENSP00000514272.1:p.Glu181Ter
|
|
ENST00000699292.1:n.456G>T
|
|
|
ENST00000225275.4:c.1416G>T
MANE Select
|
ENSP00000225275.3:p.Met472Ile
|
|
ENST00000225275.3:c.1416G>T
|
ENSP00000225275.3:p.Met472Ile
|
|
NM_000250.1:c.1416G>T , LRG_84t1:c.1416G>T
|
NP_000241.1:p.Met472Ile
|
|
XM_011524821.1:c.1602G>T
|
XP_011523123.1:p.Met534Ile
|
|
XM_011524822.1:c.1131G>T
|
XP_011523124.1:p.Met377Ile
|
|
XM_011524823.1:c.1441G>T
|
XP_011523125.1:p.Glu481Ter
|
|
NM_000250.2:c.1416G>T
MANE Select
|
NP_000241.1:p.Met472Ile
|
|