ENST00000578493.2:n.709A>G
|
|
|
ENST00000699291.1:c.501A>G
|
ENSP00000514272.1:p.Leu167=
|
|
ENST00000699292.1:n.416A>G
|
|
|
ENST00000225275.4:c.1376A>G
MANE Select
|
ENSP00000225275.3:p.Tyr459Cys
|
|
ENST00000225275.3:c.1376A>G
|
ENSP00000225275.3:p.Tyr459Cys
|
|
NM_000250.1:c.1376A>G , LRG_84t1:c.1376A>G
|
NP_000241.1:p.Tyr459Cys
|
|
XM_011524821.1:c.1562A>G
|
XP_011523123.1:p.Tyr521Cys
|
|
XM_011524822.1:c.1091A>G
|
XP_011523124.1:p.Tyr364Cys
|
|
XM_011524823.1:c.1401A>G
|
XP_011523125.1:p.Leu467=
|
|
NM_000250.2:c.1376A>G
MANE Select
|
NP_000241.1:p.Tyr459Cys
|
|