ENST00000361462.7:c.*224G>T
MANE Select
|
ENSP00000354917.2:n.*224G>T
|
|
ENST00000361462.6:c.*224G>T
|
ENSP00000354917.2:n.*224G>T
|
|
ENST00000361577.7:c.*224G>T
|
ENSP00000355045.3:n.*224G>T
|
|
ENST00000556823.1:c.692G>T
|
ENSP00000450465.1:n.692G>T
|
|
ENST00000557423.5:c.*2389G>T
|
ENSP00000451829.1:n.*2389G>T
|
|
NM_001308120.1:c.*224G>T
|
NP_001295049.1:n.*224G>T
|
|
NM_015091.2:c.*224G>T
|
NP_055906.2:n.*224G>T
|
|
NM_015091.3:c.*224G>T
|
NP_055906.2:n.*224G>T
|
|
NR_131765.1:n.5609G>T
|
|
|
XM_011536571.1:c.*529G>T
|
XP_011534873.1:n.*529G>T
|
|
XM_017021098.1:c.*224G>T
|
XP_016876587.1:n.*224G>T
|
|
XM_017021099.1:c.*224G>T
|
XP_016876588.1:n.*224G>T
|
|
XR_001750194.1:n.5873G>T
|
|
|
XR_001750195.1:n.5516G>T
|
|
|
NM_001308120.2:c.*224G>T
MANE Select
|
NP_001295049.1:n.*224G>T
|
|
NM_015091.4:c.*224G>T
|
NP_055906.2:n.*224G>T
|
|
NR_131765.2:n.5609G>T
|
|
|