ENST00000339818.9:c.357G=
MANE Select
|
ENSP00000344566.4:p.Gln119=
|
|
ENST00000325223.7:c.357G=
|
ENSP00000317302.7:p.Gln119=
|
|
ENST00000339818.8:c.357G=
|
ENSP00000344566.4:p.Gln119=
|
|
ENST00000397956.7:c.357G=
|
ENSP00000381047.3:p.Gln119=
|
|
ENST00000462742.1:n.2528G=
|
|
|
ENST00000478674.1:n.416G=
|
|
|
ENST00000496321.5:n.473G=
|
|
|
NM_001271440.1:c.357G=
|
NP_001258369.1:p.Gln119=
|
|
NM_001271441.1:c.357G=
|
NP_001258370.1:p.Gln119=
|
|
NM_001271442.1:c.234G=
|
NP_001258371.1:p.Gln78=
|
|
NM_004928.2:c.357G=
|
NP_004919.1:p.Gln119=
|
|
XM_006724051.2:c.432G=
|
XP_006724114.1:p.Gln144=
|
|
XM_006724052.2:c.432G=
|
XP_006724115.1:p.Gln144=
|
|
XM_006724053.2:c.33G=
|
XP_006724116.1:p.Gln11=
|
|
XR_937571.1:n.560G=
|
|
|
XM_006724051.3:c.432G=
|
XP_006724114.1:p.Gln144=
|
|
XM_006724053.3:c.33G=
|
XP_006724116.1:p.Gln11=
|
|
XM_017028470.1:c.561G=
|
XP_016883959.1:p.Gln187=
|
|
XM_017028471.1:c.306G=
|
XP_016883960.1:p.Gln102=
|
|
XM_017028472.1:c.33G=
|
XP_016883961.1:p.Gln11=
|
|
XR_937571.2:n.567G=
|
|
|
NM_004928.3:c.357G=
MANE Select
|
NP_004919.1:p.Gln119=
|
|
NM_001271440.2:c.357G=
|
NP_001258369.1:p.Gln119=
|
|
NM_001271441.2:c.357G=
|
NP_001258370.1:p.Gln119=
|
|