ENST00000366971.9:c.368T>A
MANE Select
|
ENSP00000355938.4:p.Phe123Tyr
|
|
ENST00000366971.8:c.368T>A
|
ENSP00000355938.4:p.Phe123Tyr
|
|
NM_014053.3:c.368T>A
|
NP_054772.1:p.Phe123Tyr
|
|
XM_011509446.1:c.368T>A
|
XP_011507748.1:p.Phe123Tyr
|
|
XM_011509447.1:c.368T>A
|
XP_011507749.1:p.Phe123Tyr
|
|
XM_011509448.1:c.368T>A
|
XP_011507750.1:p.Phe123Tyr
|
|
XR_247024.1:n.542T>A
|
|
|
XR_426771.1:n.542T>A
|
|
|
XR_426772.2:n.542T>A
|
|
|
XR_921769.1:n.542T>A
|
|
|
XM_011509446.3:c.368T>A
|
XP_011507748.1:p.Phe123Tyr
|
|
XM_011509447.2:c.368T>A
|
XP_011507749.1:p.Phe123Tyr
|
|
XR_247024.3:n.542T>A
|
|
|
XR_426772.3:n.542T>A
|
|
|
NM_014053.4:c.368T>A
MANE Select
|
NP_054772.1:p.Phe123Tyr
|
|