ENST00000339818.9:c.227G>C
MANE Select
|
ENSP00000344566.4:p.Ser76Thr
|
|
ENST00000325223.7:c.227G>C
|
ENSP00000317302.7:p.Ser76Thr
|
|
ENST00000339818.8:c.227G>C
|
ENSP00000344566.4:p.Ser76Thr
|
|
ENST00000397956.7:c.227G>C
|
ENSP00000381047.3:p.Ser76Thr
|
|
ENST00000462742.1:n.2398G>C
|
|
|
ENST00000478674.1:n.286G>C
|
|
|
ENST00000496321.5:n.343G>C
|
|
|
NM_001271440.1:c.227G>C
|
NP_001258369.1:p.Ser76Thr
|
|
NM_001271441.1:c.227G>C
|
NP_001258370.1:p.Ser76Thr
|
|
NM_001271442.1:c.104G>C
|
NP_001258371.1:p.Ser35Thr
|
|
NM_004928.2:c.227G>C
|
NP_004919.1:p.Ser76Thr
|
|
XM_006724051.2:c.302G>C
|
XP_006724114.1:p.Ser101Thr
|
|
XM_006724052.2:c.302G>C
|
XP_006724115.1:p.Ser101Thr
|
|
XM_006724053.2:c.-98G>C
|
XP_006724116.1:n.-98G>C
|
|
XR_937571.1:n.430G>C
|
|
|
XM_006724051.3:c.302G>C
|
XP_006724114.1:p.Ser101Thr
|
|
XM_006724053.3:c.-98G>C
|
XP_006724116.1:n.-98G>C
|
|
XM_017028470.1:c.431G>C
|
XP_016883959.1:p.Ser144Thr
|
|
XM_017028471.1:c.176G>C
|
XP_016883960.1:p.Ser59Thr
|
|
XM_017028472.1:c.-98G>C
|
XP_016883961.1:n.-98G>C
|
|
XR_937571.2:n.437G>C
|
|
|
NM_004928.3:c.227G>C
MANE Select
|
NP_004919.1:p.Ser76Thr
|
|
NM_001271440.2:c.227G>C
|
NP_001258369.1:p.Ser76Thr
|
|
NM_001271441.2:c.227G>C
|
NP_001258370.1:p.Ser76Thr
|
|