ENST00000578493.2:n.732C>G
|
|
|
ENST00000699291.1:c.524C>G
|
ENSP00000514272.1:p.Ala175Gly
|
|
ENST00000699292.1:n.439C>G
|
|
|
ENST00000225275.4:c.1399C>G
MANE Select
|
ENSP00000225275.3:p.Leu467Val
|
|
ENST00000225275.3:c.1399C>G
|
ENSP00000225275.3:p.Leu467Val
|
|
NM_000250.1:c.1399C>G , LRG_84t1:c.1399C>G
|
NP_000241.1:p.Leu467Val
|
|
XM_011524821.1:c.1585C>G
|
XP_011523123.1:p.Leu529Val
|
|
XM_011524822.1:c.1114C>G
|
XP_011523124.1:p.Leu372Val
|
|
XM_011524823.1:c.1424C>G
|
XP_011523125.1:p.Ala475Gly
|
|
NM_000250.2:c.1399C>G
MANE Select
|
NP_000241.1:p.Leu467Val
|
|