ENST00000298910.12:c.4219C>T
MANE Select
|
ENSP00000298910.7:p.His1407Tyr
|
|
ENST00000679360.1:c.*3128C>T
|
ENSP00000505368.1:n.*3128C>T
|
|
ENST00000680790.1:c.3964C>T
|
ENSP00000505335.1:p.His1322Tyr
|
|
ENST00000298910.11:c.4219C>T
|
ENSP00000298910.7:p.His1407Tyr
|
|
ENST00000430804.5:c.1515C>T
|
|
|
ENST00000479187.5:n.900C>T
|
|
|
NM_198578.3:c.4219C>T
|
NP_940980.3:p.His1407Tyr
|
|
XM_005268629.2:c.4219C>T
|
XP_005268686.1:p.His1407Tyr
|
|
XM_011537877.1:c.4219C>T
|
XP_011536179.1:p.His1407Tyr
|
|
XM_011537878.1:c.4219C>T
|
XP_011536180.1:p.His1407Tyr
|
|
XM_011537879.1:c.3016C>T
|
XP_011536181.1:p.His1006Tyr
|
|
XM_011537880.1:c.4219C>T
|
XP_011536182.1:p.His1407Tyr
|
|
XM_011537881.1:c.4219C>T
|
XP_011536183.1:p.His1407Tyr
|
|
XM_005268629.4:c.4219C>T
|
XP_005268686.1:p.His1407Tyr
|
|
XM_011537877.3:c.4219C>T
|
XP_011536179.1:p.His1407Tyr
|
|
XM_011537881.3:c.4219C>T
|
XP_011536183.1:p.His1407Tyr
|
|
XM_017018786.2:c.4219C>T
|
XP_016874275.1:p.His1407Tyr
|
|
XM_017018787.1:c.1135C>T
|
XP_016874276.1:p.His379Tyr
|
|
XM_017018788.2:c.481C>T
|
XP_016874277.1:p.His161Tyr
|
|
XM_024448833.1:c.3016C>T
|
XP_024304601.1:p.His1006Tyr
|
|
XR_001748574.2:n.4461C>T
|
|
|
NM_198578.4:c.4219C>T
MANE Select
|
NP_940980.4:p.His1407Tyr
|
|