ENST00000700012.1:c.544C>T
|
ENSP00000514753.1:p.His182Tyr
|
|
ENST00000700013.1:c.544C>T
|
ENSP00000514754.1:p.His182Tyr
|
|
ENST00000700114.1:c.466C>T
|
ENSP00000514808.1:p.His156Tyr
|
|
ENST00000700115.1:c.526C>T
|
ENSP00000514809.1:p.His176Tyr
|
|
ENST00000700118.1:c.526C>T
|
ENSP00000514810.1:p.His176Tyr
|
|
ENST00000700119.1:c.*337C>T
|
ENSP00000514811.1:n.*337C>T
|
|
ENST00000700120.1:n.454C>T
|
|
|
ENST00000275034.5:c.526C>T
MANE Select
|
ENSP00000275034.3:p.His176Tyr
|
|
ENST00000275034.4:c.526C>T
|
ENSP00000275034.3:p.His176Tyr
|
|
NM_017934.5:c.526C>T
|
NP_060404.3:p.His176Tyr
|
|
XM_005248729.3:c.526C>T
|
XP_005248786.1:p.His176Tyr
|
|
XM_011535917.1:c.526C>T
|
XP_011534219.1:p.His176Tyr
|
|
XM_011535918.1:c.10C>T
|
XP_011534220.1:p.His4Tyr
|
|
XM_011535919.1:c.526C>T
|
XP_011534221.1:p.His176Tyr
|
|
XR_942499.1:n.752C>T
|
|
|
NM_017934.6:c.526C>T
|
NP_060404.4:p.His176Tyr
|
|
XM_005248729.5:c.526C>T
|
XP_005248786.1:p.His176Tyr
|
|
XM_011535918.3:c.10C>T
|
XP_011534220.1:p.His4Tyr
|
|
XM_017010989.2:c.-1204C>T
|
XP_016866478.1:n.-1204C>T
|
|
XM_017010990.2:c.-1204C>T
|
XP_016866479.1:n.-1204C>T
|
|
NM_017934.7:c.526C>T
MANE Select
|
NP_060404.4:p.His176Tyr
|
|