ENST00000298910.12:c.7031T>A
MANE Select
|
ENSP00000298910.7:p.Phe2344Tyr
|
|
ENST00000636518.1:c.828T>A
|
|
|
ENST00000679360.1:c.*5940T>A
|
ENSP00000505368.1:n.*5940T>A
|
|
ENST00000679532.1:c.2805T>A
|
|
|
ENST00000679683.1:c.821T>A
|
|
|
ENST00000680018.1:c.2476T>A
|
ENSP00000505347.1:n.2476T>A
|
|
ENST00000680422.1:c.4118T>A
|
|
|
ENST00000680425.1:c.2198T>A
|
ENSP00000506459.1:n.2198T>A
|
|
ENST00000680453.1:c.2488T>A
|
|
|
ENST00000680790.1:c.6776T>A
|
ENSP00000505335.1:p.Phe2259Tyr
|
|
ENST00000681136.1:n.3015T>A
|
|
|
ENST00000681696.1:c.2714T>A
|
ENSP00000505871.1:p.Phe905Tyr
|
|
ENST00000681773.1:n.238T>A
|
|
|
ENST00000298910.11:c.7031T>A
|
ENSP00000298910.7:p.Phe2344Tyr
|
|
ENST00000430804.5:c.4327T>A
|
|
|
ENST00000479187.5:n.3712T>A
|
|
|
NM_198578.3:c.7031T>A
|
NP_940980.3:p.Phe2344Tyr
|
|
XM_005268629.2:c.7031T>A
|
XP_005268686.1:p.Phe2344Tyr
|
|
XM_011537877.1:c.7031T>A
|
XP_011536179.1:p.Phe2344Tyr
|
|
XM_011537879.1:c.5828T>A
|
XP_011536181.1:p.Phe1943Tyr
|
|
XR_944868.1:n.485-8577A>T
|
|
|
XM_005268629.4:c.7031T>A
|
XP_005268686.1:p.Phe2344Tyr
|
|
XM_011537877.3:c.7031T>A
|
XP_011536179.1:p.Phe2344Tyr
|
|
XM_017018787.1:c.3947T>A
|
XP_016874276.1:p.Phe1316Tyr
|
|
XM_017018788.2:c.3293T>A
|
XP_016874277.1:p.Phe1098Tyr
|
|
XM_024448833.1:c.5828T>A
|
XP_024304601.1:p.Phe1943Tyr
|
|
XR_944868.2:n.485-8577A>T
|
|
|
NM_198578.4:c.7031T>A
MANE Select
|
NP_940980.4:p.Phe2344Tyr
|
|