ENST00000262367.10:c.4555T>C
MANE Select
|
ENSP00000262367.5:p.Tyr1519His
|
|
ENST00000262367.9:c.4555T>C
|
ENSP00000262367.5:p.Tyr1519His
|
|
ENST00000382070.7:c.4441T>C
|
ENSP00000371502.3:p.Tyr1481His
|
|
ENST00000570939.2:c.3190T>C
|
ENSP00000461002.2:p.Tyr1064His
|
|
ENST00000571763.5:n.345T>C
|
|
|
ENST00000574740.1:n.376T>C
|
|
|
ENST00000576720.1:n.3378T>C
|
|
|
NM_001079846.1:c.4441T>C
|
NP_001073315.1:p.Tyr1481His
|
|
NM_004380.2:c.4555T>C
|
NP_004371.2:p.Tyr1519His
|
|
XM_005255124.3:c.4510T>C
|
XP_005255181.1:p.Tyr1504His
|
|
XM_005255125.3:c.4138T>C
|
XP_005255182.1:p.Tyr1380His
|
|
XM_006720848.2:c.4294T>C
|
XP_006720911.1:p.Tyr1432His
|
|
XM_011522380.1:c.4501T>C
|
XP_011520682.1:p.Tyr1501His
|
|
XM_011522381.1:c.3802T>C
|
XP_011520683.1:p.Tyr1268His
|
|
XM_005255124.4:c.4510T>C
|
XP_005255181.1:p.Tyr1504His
|
|
XM_005255125.4:c.4138T>C
|
XP_005255182.1:p.Tyr1380His
|
|
XM_006720848.3:c.4294T>C
|
XP_006720911.1:p.Tyr1432His
|
|
XM_011522381.2:c.3802T>C
|
XP_011520683.1:p.Tyr1268His
|
|
XM_017022944.1:c.4549T>C
|
XP_016878433.1:p.Tyr1517His
|
|
NM_004380.3:c.4555T>C
MANE Select
|
NP_004371.2:p.Tyr1519His
|
|