ENST00000261647.10:c.168G>T
MANE Select
|
ENSP00000261647.5:p.Leu56=
|
|
ENST00000261647.9:c.168G>T
|
ENSP00000261647.5:p.Leu56=
|
|
ENST00000466729.5:c.233G>T
|
|
|
ENST00000470399.1:c.183G>T
|
ENSP00000465082.1:p.Leu61=
|
|
ENST00000475723.5:c.215G>T
|
|
|
ENST00000497842.6:n.193G>T
|
|
|
ENST00000583704.1:n.193G>T
|
|
|
NM_001271420.1:c.-291G>T
|
NP_001258349.1:n.-291G>T
|
|
NM_017775.3:c.168G>T
|
NP_060245.3:p.Leu56=
|
|
XM_011523950.1:c.168G>T
|
XP_011522252.1:p.Leu56=
|
|
XM_017024801.2:c.168G>T
|
XP_016880290.2:p.Leu56=
|
|
XM_017024802.2:c.168G>T
|
XP_016880291.2:p.Leu56=
|
|
XM_024450814.1:c.168G>T
|
XP_024306582.1:p.Leu56=
|
|
NM_017775.4:c.168G>T
MANE Select
|
NP_060245.3:p.Leu56=
|
|
NM_001271420.2:c.-291G>T
|
NP_001258349.1:n.-291G>T
|
|