ENST00000298910.12:c.7042G>A
MANE Select
|
ENSP00000298910.7:p.Ala2348Thr
|
|
ENST00000636518.1:c.839G>A
|
|
|
ENST00000679360.1:c.*5951G>A
|
ENSP00000505368.1:n.*5951G>A
|
|
ENST00000679532.1:c.2816G>A
|
|
|
ENST00000679683.1:c.832G>A
|
|
|
ENST00000680018.1:c.2487G>A
|
ENSP00000505347.1:n.2487G>A
|
|
ENST00000680422.1:c.4129G>A
|
|
|
ENST00000680425.1:c.2209G>A
|
ENSP00000506459.1:n.2209G>A
|
|
ENST00000680453.1:c.2499G>A
|
|
|
ENST00000680790.1:c.6787G>A
|
ENSP00000505335.1:p.Ala2263Thr
|
|
ENST00000681136.1:n.3026G>A
|
|
|
ENST00000681696.1:c.2725G>A
|
ENSP00000505871.1:p.Ala909Thr
|
|
ENST00000681773.1:n.249G>A
|
|
|
ENST00000298910.11:c.7042G>A
|
ENSP00000298910.7:p.Ala2348Thr
|
|
ENST00000430804.5:c.4338G>A
|
|
|
ENST00000479187.5:n.3723G>A
|
|
|
NM_198578.3:c.7042G>A
|
NP_940980.3:p.Ala2348Thr
|
|
XM_005268629.2:c.7042G>A
|
XP_005268686.1:p.Ala2348Thr
|
|
XM_011537877.1:c.7042G>A
|
XP_011536179.1:p.Ala2348Thr
|
|
XM_011537879.1:c.5839G>A
|
XP_011536181.1:p.Ala1947Thr
|
|
XR_944868.1:n.485-8588C>T
|
|
|
XM_005268629.4:c.7042G>A
|
XP_005268686.1:p.Ala2348Thr
|
|
XM_011537877.3:c.7042G>A
|
XP_011536179.1:p.Ala2348Thr
|
|
XM_017018787.1:c.3958G>A
|
XP_016874276.1:p.Ala1320Thr
|
|
XM_017018788.2:c.3304G>A
|
XP_016874277.1:p.Ala1102Thr
|
|
XM_024448833.1:c.5839G>A
|
XP_024304601.1:p.Ala1947Thr
|
|
XR_944868.2:n.485-8588C>T
|
|
|
NM_198578.4:c.7042G>A
MANE Select
|
NP_940980.4:p.Ala2348Thr
|
|