ENST00000578493.2:n.722G>T
|
|
|
ENST00000699291.1:c.514G>T
|
ENSP00000514272.1:p.Ala172Ser
|
|
ENST00000699292.1:n.429G>T
|
|
|
ENST00000225275.4:c.1389G>T
MANE Select
|
ENSP00000225275.3:p.Leu463=
|
|
ENST00000225275.3:c.1389G>T
|
ENSP00000225275.3:p.Leu463=
|
|
NM_000250.1:c.1389G>T , LRG_84t1:c.1389G>T
|
NP_000241.1:p.Leu463=
|
|
XM_011524821.1:c.1575G>T
|
XP_011523123.1:p.Leu525=
|
|
XM_011524822.1:c.1104G>T
|
XP_011523124.1:p.Leu368=
|
|
XM_011524823.1:c.1414G>T
|
XP_011523125.1:p.Ala472Ser
|
|
NM_000250.2:c.1389G>T
MANE Select
|
NP_000241.1:p.Leu463=
|
|