ENST00000339818.9:c.279G>C
MANE Select
|
ENSP00000344566.4:p.Trp93Cys
|
|
ENST00000325223.7:c.279G>C
|
ENSP00000317302.7:p.Trp93Cys
|
|
ENST00000339818.8:c.279G>C
|
ENSP00000344566.4:p.Trp93Cys
|
|
ENST00000397956.7:c.279G>C
|
ENSP00000381047.3:p.Trp93Cys
|
|
ENST00000462742.1:n.2450G>C
|
|
|
ENST00000478674.1:n.338G>C
|
|
|
ENST00000496321.5:n.395G>C
|
|
|
NM_001271440.1:c.279G>C
|
NP_001258369.1:p.Trp93Cys
|
|
NM_001271441.1:c.279G>C
|
NP_001258370.1:p.Trp93Cys
|
|
NM_001271442.1:c.156G>C
|
NP_001258371.1:p.Trp52Cys
|
|
NM_004928.2:c.279G>C
|
NP_004919.1:p.Trp93Cys
|
|
XM_006724051.2:c.354G>C
|
XP_006724114.1:p.Trp118Cys
|
|
XM_006724052.2:c.354G>C
|
XP_006724115.1:p.Trp118Cys
|
|
XM_006724053.2:c.-46G>C
|
XP_006724116.1:n.-46G>C
|
|
XR_937571.1:n.482G>C
|
|
|
XM_006724051.3:c.354G>C
|
XP_006724114.1:p.Trp118Cys
|
|
XM_006724053.3:c.-46G>C
|
XP_006724116.1:n.-46G>C
|
|
XM_017028470.1:c.483G>C
|
XP_016883959.1:p.Trp161Cys
|
|
XM_017028471.1:c.228G>C
|
XP_016883960.1:p.Trp76Cys
|
|
XM_017028472.1:c.-46G>C
|
XP_016883961.1:n.-46G>C
|
|
XR_937571.2:n.489G>C
|
|
|
NM_004928.3:c.279G>C
MANE Select
|
NP_004919.1:p.Trp93Cys
|
|
NM_001271440.2:c.279G>C
|
NP_001258369.1:p.Trp93Cys
|
|
NM_001271441.2:c.279G>C
|
NP_001258370.1:p.Trp93Cys
|
|