ENST00000682114.1:c.572+1G>T
|
ENSP00000507245.1:n.572+1G>T
|
|
ENST00000682478.1:n.762+1G>T
|
|
|
ENST00000683576.1:n.763G>T
|
|
|
ENST00000683627.1:c.573G>T
|
ENSP00000507533.1:p.Met191Ile
|
|
ENST00000684082.1:c.530G>T
|
ENSP00000508266.1:n.530G>T
|
|
ENST00000684633.1:n.545G>T
|
|
|
ENST00000684678.1:c.568+1G>T
|
ENSP00000507059.1:n.568+1G>T
|
|
ENST00000369842.9:c.573G>T
MANE Select
|
ENSP00000358857.4:p.Met191Ile
|
|
ENST00000369835.3:c.468G>T
|
ENSP00000358850.3:p.Met156Ile
|
|
ENST00000369842.8:c.573G>T
|
ENSP00000358857.4:p.Met191Ile
|
|
ENST00000428228.5:c.*478G>T
|
ENSP00000401081.1:n.*478G>T
|
|
ENST00000471965.1:n.362G>T
|
|
|
ENST00000486738.5:n.1010G>T
|
|
|
ENST00000492448.1:n.556G>T
|
|
|
NM_000117.2:c.573G>T , LRG_745t1:c.573G>T
|
NP_000108.1:p.Met191Ile
|
|
XM_024452349.1:c.579G>T
|
XP_024308117.1:p.Met193Ile
|
|
NM_000117.3:c.573G>T
MANE Select
|
NP_000108.1:p.Met191Ile
|
|