ENST00000578493.2:n.1023G>T
|
|
|
ENST00000699291.1:c.815G>T
|
ENSP00000514272.1:n.815G>T
|
|
ENST00000699292.1:n.1225G>T
|
|
|
ENST00000225275.4:c.1690G>T
MANE Select
|
ENSP00000225275.3:p.Ala564Ser
|
|
ENST00000225275.3:c.1690G>T
|
ENSP00000225275.3:p.Ala564Ser
|
|
ENST00000577220.1:c.148G>T
|
ENSP00000464668.1:p.Ala50Ser
|
|
NM_000250.1:c.1690G>T , LRG_84t1:c.1690G>T
|
NP_000241.1:p.Ala564Ser
|
|
XM_011524821.1:c.1876G>T
|
XP_011523123.1:p.Ala626Ser
|
|
XM_011524822.1:c.1405G>T
|
XP_011523124.1:p.Ala469Ser
|
|
NM_000250.2:c.1690G>T
MANE Select
|
NP_000241.1:p.Ala564Ser
|
|