ENST00000355773.6:c.382T>C
MANE Select
|
ENSP00000348019.5:p.Tyr128His
|
|
ENST00000355773.5:c.382T>C
|
ENSP00000348019.5:p.Tyr128His
|
|
ENST00000481996.1:n.148T>C
|
|
|
NM_012434.4:c.382T>C
|
NP_036566.1:p.Tyr128His
|
|
XM_005248710.2:c.331T>C
|
XP_005248767.1:p.Tyr111His
|
|
XM_005248711.1:c.184T>C
|
XP_005248768.1:p.Tyr62His
|
|
XM_011535750.1:c.382T>C
|
XP_011534052.1:p.Tyr128His
|
|
XM_011535751.1:c.382T>C
|
XP_011534053.1:p.Tyr128His
|
|
NM_012434.5:c.382T>C
MANE Select
|
NP_036566.1:p.Tyr128His
|
|
NM_001382629.1:c.151T>C
|
NP_001369558.1:p.Tyr51His
|
|
NM_001382630.1:c.382T>C
|
NP_001369559.1:p.Tyr128His
|
|
NM_001382631.1:c.403T>C
|
NP_001369560.1:p.Tyr135His
|
|
NM_001382632.1:c.382T>C
|
NP_001369561.1:p.Tyr128His
|
|
NM_001382633.1:c.382T>C
|
NP_001369562.1:p.Tyr128His
|
|
NM_001382634.1:c.382T>C
|
NP_001369563.1:p.Tyr128His
|
|
NM_001382635.1:c.382T>C
|
NP_001369564.1:p.Tyr128His
|
|
NM_001382636.1:c.151T>C
|
NP_001369565.1:p.Tyr51His
|
|