|
NM_004836.7:c.556T>C
MANE Select
|
NP_004827.4:p.Tyr186His
|
|
ENST00000303236.9:c.556T>C
MANE Select
|
ENSP00000307235.3:p.Tyr186His
|
|
NM_001313915.1:c.103T>C
|
NP_001300844.1:p.Tyr35His
|
|
NM_001313915.2:c.103T>C
|
NP_001300844.1:p.Tyr35His
|
|
NM_004836.5:c.556T>C
|
NP_004827.4:p.Tyr186His
|
|
NM_004836.6:c.556T>C
|
NP_004827.4:p.Tyr186His
|
|
ENST00000303236.7:c.556T>C
|
ENSP00000307235.3:p.Tyr186His
|
|
ENST00000415570.1:c.193T>C
|
ENSP00000412076.1:p.Tyr65His
|
|
ENST00000419748.5:c.103T>C
|
ENSP00000408325.1:p.Tyr35His
|
|
ENST00000652099.1:c.554T>C
|
|
|
ENST00000652736.1:n.432T>C
|
|
|
ENST00000682276.1:n.11T>C
|
|
|
ENST00000682892.1:c.103T>C
|
ENSP00000507214.1:p.Tyr35His
|
|
XM_017005376.2:c.-325T>C
|
XP_016860865.1:n.-325T>C
|
|
XR_939749.1:n.765T>C
|
|