ENST00000682114.1:c.-46G>T
|
ENSP00000507245.1:n.-46G>T
|
|
ENST00000369842.9:c.-46G>T
MANE Select
|
ENSP00000358857.4:n.-46G>T
|
|
ENST00000369835.3:c.-46G>T
|
ENSP00000358850.3:n.-46G>T
|
|
ENST00000369842.8:c.-46G>T
|
ENSP00000358857.4:n.-46G>T
|
|
ENST00000428228.5:c.-46G>T
|
ENSP00000401081.1:n.-46G>T
|
|
ENST00000485261.1:n.36G>T
|
|
|
ENST00000486738.5:n.99G>T
|
|
|
ENST00000494443.5:n.12G>T
|
|
|
NM_000117.2:c.-46G>T , LRG_745t1:c.-46G>T
|
NP_000108.1:n.-46G>T
|
|
XM_024452349.1:c.-254G>T
|
XP_024308117.1:n.-254G>T
|
|
NM_000117.3:c.-46G>T
MANE Select
|
NP_000108.1:n.-46G>T
|
|