ENST00000682114.1:c.219G>T
|
ENSP00000507245.1:p.Met73Ile
|
|
ENST00000682478.1:n.195G>T
|
|
|
ENST00000683576.1:n.195G>T
|
|
|
ENST00000683627.1:c.219G>T
|
ENSP00000507533.1:p.Met73Ile
|
|
ENST00000684082.1:c.219G>T
|
ENSP00000508266.1:p.Met73Ile
|
|
ENST00000684633.1:n.191G>T
|
|
|
ENST00000684678.1:c.215G>T
|
ENSP00000507059.1:n.215G>T
|
|
ENST00000369842.9:c.219G>T
MANE Select
|
ENSP00000358857.4:p.Met73Ile
|
|
ENST00000369835.3:c.114G>T
|
ENSP00000358850.3:p.Met38Ile
|
|
ENST00000369842.8:c.219G>T
|
ENSP00000358857.4:p.Met73Ile
|
|
ENST00000428228.5:c.*124G>T
|
ENSP00000401081.1:n.*124G>T
|
|
ENST00000468294.5:n.179G>T
|
|
|
ENST00000485261.1:n.195G>T
|
|
|
ENST00000486738.5:n.363G>T
|
|
|
ENST00000492448.1:n.202G>T
|
|
|
ENST00000494443.5:n.276G>T
|
|
|
NM_000117.2:c.219G>T , LRG_745t1:c.219G>T
|
NP_000108.1:p.Met73Ile
|
|
XM_024452349.1:c.11G>T
|
XP_024308117.1:p.Cys4Phe
|
|
NM_000117.3:c.219G>T
MANE Select
|
NP_000108.1:p.Met73Ile
|
|