ENST00000545712.7:c.200T>A
MANE Select
|
ENSP00000445920.1:p.Phe67Tyr
|
|
ENST00000420167.6:c.*29T>A
|
ENSP00000416136.2:n.*29T>A
|
|
ENST00000503497.7:c.200T>A
|
ENSP00000474881.1:p.Phe67Tyr
|
|
ENST00000536760.1:n.203T>A
|
|
|
ENST00000537236.2:c.200T>A
|
ENSP00000483818.1:p.Phe67Tyr
|
|
ENST00000537496.5:c.200T>A
|
ENSP00000444793.1:p.Phe67Tyr
|
|
ENST00000540016.5:c.135-3684T>A
|
ENSP00000474582.1:n.135-3684T>A
|
|
ENST00000541763.6:c.200T>A
|
ENSP00000474981.1:p.Phe67Tyr
|
|
ENST00000542390.5:n.227T>A
|
|
|
ENST00000544051.5:c.138T>A
|
ENSP00000438079.1:p.Val46=
|
|
ENST00000545712.6:c.200T>A
|
ENSP00000445920.1:p.Phe67Tyr
|
|
NM_052845.3:c.200T>A
|
NP_443077.1:p.Phe67Tyr
|
|
NR_038118.1:n.273T>A
|
|
|
XM_024448961.1:c.200T>A
|
XP_024304729.1:p.Phe67Tyr
|
|
NM_052845.4:c.200T>A
MANE Select
|
NP_443077.1:p.Phe67Tyr
|
|
NR_038118.2:n.224T>A
|
|
|