ENST00000339818.9:c.369C>T
MANE Select
|
ENSP00000344566.4:p.Asn123=
|
|
ENST00000325223.7:c.369C>T
|
ENSP00000317302.7:p.Asn123=
|
|
ENST00000339818.8:c.369C>T
|
ENSP00000344566.4:p.Asn123=
|
|
ENST00000397956.7:c.369C>T
|
ENSP00000381047.3:p.Asn123=
|
|
ENST00000462742.1:n.2540C>T
|
|
|
ENST00000478674.1:n.428C>T
|
|
|
ENST00000496321.5:n.485C>T
|
|
|
NM_001271440.1:c.369C>T
|
NP_001258369.1:p.Asn123=
|
|
NM_001271441.1:c.369C>T
|
NP_001258370.1:p.Asn123=
|
|
NM_001271442.1:c.246C>T
|
NP_001258371.1:p.Asn82=
|
|
NM_004928.2:c.369C>T
|
NP_004919.1:p.Asn123=
|
|
XM_006724051.2:c.444C>T
|
XP_006724114.1:p.Asn148=
|
|
XM_006724052.2:c.444C>T
|
XP_006724115.1:p.Asn148=
|
|
XM_006724053.2:c.45C>T
|
XP_006724116.1:p.Asn15=
|
|
XR_937571.1:n.572C>T
|
|
|
XM_006724051.3:c.444C>T
|
XP_006724114.1:p.Asn148=
|
|
XM_006724053.3:c.45C>T
|
XP_006724116.1:p.Asn15=
|
|
XM_017028470.1:c.573C>T
|
XP_016883959.1:p.Asn191=
|
|
XM_017028471.1:c.318C>T
|
XP_016883960.1:p.Asn106=
|
|
XM_017028472.1:c.45C>T
|
XP_016883961.1:p.Asn15=
|
|
XR_937571.2:n.579C>T
|
|
|
NM_004928.3:c.369C>T
MANE Select
|
NP_004919.1:p.Asn123=
|
|
NM_001271440.2:c.369C>T
|
NP_001258369.1:p.Asn123=
|
|
NM_001271441.2:c.369C>T
|
NP_001258370.1:p.Asn123=
|
|