ENST00000261647.10:c.126G>T
MANE Select
|
ENSP00000261647.5:p.Val42=
|
|
ENST00000261647.9:c.126G>T
|
ENSP00000261647.5:p.Val42=
|
|
ENST00000466729.5:c.191G>T
|
|
|
ENST00000470399.1:c.141G>T
|
ENSP00000465082.1:p.Val47=
|
|
ENST00000475723.5:c.173G>T
|
|
|
ENST00000497842.6:n.151G>T
|
|
|
ENST00000583704.1:n.151G>T
|
|
|
NM_001271420.1:c.-333G>T
|
NP_001258349.1:n.-333G>T
|
|
NM_017775.3:c.126G>T
|
NP_060245.3:p.Val42=
|
|
XM_011523950.1:c.126G>T
|
XP_011522252.1:p.Val42=
|
|
XM_017024801.2:c.126G>T
|
XP_016880290.2:p.Val42=
|
|
XM_017024802.2:c.126G>T
|
XP_016880291.2:p.Val42=
|
|
XM_024450814.1:c.126G>T
|
XP_024306582.1:p.Val42=
|
|
NM_017775.4:c.126G>T
MANE Select
|
NP_060245.3:p.Val42=
|
|
NM_001271420.2:c.-333G>T
|
NP_001258349.1:n.-333G>T
|
|