ENST00000261643.8:c.527G>T
MANE Select
|
ENSP00000261643.3:p.Gly176Val
|
|
ENST00000664217.1:c.527G>T
|
ENSP00000499396.1:p.Gly176Val
|
|
ENST00000670279.1:c.527G>T
|
ENSP00000499450.1:p.Gly176Val
|
|
ENST00000261643.7:c.527G>T
|
ENSP00000261643.3:p.Gly176Val
|
|
ENST00000580561.1:c.*16G>T
|
ENSP00000462190.1:n.*16G>T
|
|
ENST00000581931.5:c.499+25089G>T
|
ENSP00000462512.1:n.499+25089G>T
|
|
NM_001303.3:c.527G>T
|
NP_001294.2:p.Gly176Val
|
|
XM_005256458.1:c.527G>T
|
XP_005256515.1:p.Gly176Val
|
|
XM_011523657.1:c.527G>T
|
XP_011521959.1:p.Gly176Val
|
|
XM_011523658.1:c.48+25089G>T
|
XP_011521960.1:n.48+25089G>T
|
|
XR_933974.1:n.630G>T
|
|
|
XR_933975.1:n.630G>T
|
|
|
NM_001303.4:c.527G>T
MANE Select
|
NP_001294.2:p.Gly176Val
|
|