ENST00000703783.1:n.349C>T
|
|
|
ENST00000703785.1:n.430C>T
|
|
|
ENST00000262464.9:c.3565C>T
MANE Select
|
ENSP00000262464.4:p.His1189Tyr
|
|
ENST00000262464.8:c.3565C>T
|
ENSP00000262464.4:p.His1189Tyr
|
|
ENST00000507835.5:c.115C>T
|
ENSP00000426839.1:p.His39Tyr
|
|
ENST00000508053.5:c.3565C>T
|
ENSP00000424571.1:p.His1189Tyr
|
|
ENST00000508989.5:c.3466C>T
|
ENSP00000425596.1:p.His1156Tyr
|
|
ENST00000619499.4:c.3562C>T
|
ENSP00000482132.1:p.His1188Tyr
|
|
NM_001999.3:c.3565C>T
|
NP_001990.2:p.His1189Tyr
|
|
XM_017009228.2:c.3412C>T
|
XP_016864717.1:p.His1138Tyr
|
|
NM_001999.4:c.3565C>T
MANE Select
|
NP_001990.2:p.His1189Tyr
|
|