ENST00000578493.2:n.1017C>T
|
|
|
ENST00000699291.1:c.809C>T
|
ENSP00000514272.1:n.809C>T
|
|
ENST00000699292.1:n.1219C>T
|
|
|
ENST00000225275.4:c.1684C>T
MANE Select
|
ENSP00000225275.3:p.Gln562Ter
|
|
ENST00000225275.3:c.1684C>T
|
ENSP00000225275.3:p.Gln562Ter
|
|
ENST00000577220.1:c.142C>T
|
ENSP00000464668.1:p.Gln48Ter
|
|
NM_000250.1:c.1684C>T , LRG_84t1:c.1684C>T
|
NP_000241.1:p.Gln562Ter
|
|
XM_011524821.1:c.1870C>T
|
XP_011523123.1:p.Gln624Ter
|
|
XM_011524822.1:c.1399C>T
|
XP_011523124.1:p.Gln467Ter
|
|
NM_000250.2:c.1684C>T
MANE Select
|
NP_000241.1:p.Gln562Ter
|
|