ENST00000354638.8:c.2278G>T
MANE Select
|
ENSP00000346659.3:p.Glu760Ter
|
|
ENST00000353809.9:c.2206G>T
|
ENSP00000261276.8:p.Glu736Ter
|
|
ENST00000354638.7:c.2278G>T
|
ENSP00000346659.3:p.Glu760Ter
|
|
NM_000275.2:c.2278G>T
|
NP_000266.2:p.Glu760Ter
|
|
NM_001300984.1:c.2206G>T
|
NP_001287913.1:p.Glu736Ter
|
|
XM_011521639.1:c.2344G>T
|
XP_011519941.1:p.Glu782Ter
|
|
XM_011521640.1:c.2320G>T
|
XP_011519942.1:p.Glu774Ter
|
|
XM_011521641.1:c.2302G>T
|
XP_011519943.1:p.Glu768Ter
|
|
XM_011521642.1:c.2272G>T
|
XP_011519944.1:p.Glu758Ter
|
|
XM_011521643.1:c.2230G>T
|
XP_011519945.1:p.Glu744Ter
|
|
XM_011521644.1:c.2206G>T
|
XP_011519946.1:p.Glu736Ter
|
|
XM_011521645.1:c.2137G>T
|
XP_011519947.1:p.Glu713Ter
|
|
XM_011521640.2:c.2320G>T
|
XP_011519942.1:p.Glu774Ter
|
|
XM_017022255.1:c.2344G>T
|
XP_016877744.1:p.Glu782Ter
|
|
XM_017022256.1:c.2302G>T
|
XP_016877745.1:p.Glu768Ter
|
|
XM_017022257.1:c.2272G>T
|
XP_016877746.1:p.Glu758Ter
|
|
XM_017022258.1:c.2302G>T
|
XP_016877747.1:p.Glu768Ter
|
|
XM_017022259.1:c.2230G>T
|
XP_016877748.1:p.Glu744Ter
|
|
XM_017022260.1:c.2206G>T
|
XP_016877749.1:p.Glu736Ter
|
|
XM_017022261.1:c.2149G>T
|
XP_016877750.1:p.Glu717Ter
|
|
XM_017022262.1:c.2268+19712G>T
|
XP_016877751.1:n.2268+19712G>T
|
|
XM_017022263.1:c.2137G>T
|
XP_016877752.1:p.Glu713Ter
|
|
XM_017022264.1:c.2137G>T
|
XP_016877753.1:p.Glu713Ter
|
|
NM_000275.3:c.2278G>T
MANE Select
|
NP_000266.2:p.Glu760Ter
|
|
NM_001300984.2:c.2206G>T
|
NP_001287913.1:p.Glu736Ter
|
|