ENST00000339818.9:c.182G>T
MANE Select
|
ENSP00000344566.4:p.Cys61Phe
|
|
ENST00000325223.7:c.182G>T
|
ENSP00000317302.7:p.Cys61Phe
|
|
ENST00000339818.8:c.182G>T
|
ENSP00000344566.4:p.Cys61Phe
|
|
ENST00000397956.7:c.182G>T
|
ENSP00000381047.3:p.Cys61Phe
|
|
ENST00000462742.1:n.2353G>T
|
|
|
ENST00000478674.1:n.241G>T
|
|
|
ENST00000496321.5:n.298G>T
|
|
|
NM_001271440.1:c.182G>T
|
NP_001258369.1:p.Cys61Phe
|
|
NM_001271441.1:c.182G>T
|
NP_001258370.1:p.Cys61Phe
|
|
NM_001271442.1:c.59G>T
|
NP_001258371.1:p.Cys20Phe
|
|
NM_004928.2:c.182G>T
|
NP_004919.1:p.Cys61Phe
|
|
XM_006724051.2:c.257G>T
|
XP_006724114.1:p.Cys86Phe
|
|
XM_006724052.2:c.257G>T
|
XP_006724115.1:p.Cys86Phe
|
|
XM_006724053.2:c.-143G>T
|
XP_006724116.1:n.-143G>T
|
|
XR_937571.1:n.385G>T
|
|
|
XM_006724051.3:c.257G>T
|
XP_006724114.1:p.Cys86Phe
|
|
XM_006724053.3:c.-143G>T
|
XP_006724116.1:n.-143G>T
|
|
XM_017028470.1:c.386G>T
|
XP_016883959.1:p.Cys129Phe
|
|
XM_017028471.1:c.131G>T
|
XP_016883960.1:p.Cys44Phe
|
|
XM_017028472.1:c.-143G>T
|
XP_016883961.1:n.-143G>T
|
|
XR_937571.2:n.392G>T
|
|
|
NM_004928.3:c.182G>T
MANE Select
|
NP_004919.1:p.Cys61Phe
|
|
NM_001271440.2:c.182G>T
|
NP_001258369.1:p.Cys61Phe
|
|
NM_001271441.2:c.182G>T
|
NP_001258370.1:p.Cys61Phe
|
|