ENST00000324324.12:c.*7981G>T
(MYEF2)
MANE Select
|
ENSP00000316950.7:n.*7981G>T
|
|
ENST00000341459.8:c.533C>A
(SLC24A5)
MANE Select
|
ENSP00000341550.3:p.Ala178Glu
|
|
ENST00000324324.11:c.*7981G>T
(MYEF2)
|
ENSP00000316950.7:n.*7981G>T
|
|
ENST00000341459.7:c.533C>A
(SLC24A5)
|
ENSP00000341550.3:p.Ala178Glu
|
|
ENST00000449382.2:c.353C>A
(SLC24A5)
|
ENSP00000389966.2:p.Ala118Glu
|
|
ENST00000463289.1:n.293C>A
(SLC24A5)
|
|
|
NM_205850.2:c.533C>A
(SLC24A5)
|
NP_995322.1:p.Ala178Glu
|
|
XM_011521458.1:c.554C>A
(SLC24A5)
|
XP_011519760.1:p.Ala185Glu
|
|
XM_005254425.4:c.*8136G>T
(MYEF2)
|
XP_005254482.2:n.*8136G>T
|
|
XM_017022079.1:c.287C>A
(SLC24A5)
|
XP_016877568.1:p.Ala96Glu
|
|
XM_017022080.1:c.287C>A
(SLC24A5)
|
XP_016877569.1:p.Ala96Glu
|
|
XM_017022285.1:c.*8136G>T
(MYEF2)
|
XP_016877774.1:n.*8136G>T
|
|
XM_017022286.1:c.*8136G>T
(MYEF2)
|
XP_016877775.1:n.*8136G>T
|
|
XM_017022287.1:c.*8136G>T
(MYEF2)
|
XP_016877776.1:n.*8136G>T
|
|
XM_017022291.1:c.*8136G>T
(MYEF2)
|
XP_016877780.1:n.*8136G>T
|
|
XM_017022292.1:c.*8136G>T
(MYEF2)
|
XP_016877781.1:n.*8136G>T
|
|
XM_024449901.1:c.194C>A
(SLC24A5)
|
XP_024305669.1:p.Ala65Glu
|
|
NM_016132.5:c.*7981G>T
(MYEF2)
MANE Select
|
NP_057216.3:n.*7981G>T
|
|
NM_001301210.2:c.*7981G>T
(MYEF2)
|
NP_001288139.2:n.*7981G>T
|
|
NM_205850.3:c.533C>A
(SLC24A5)
MANE Select
|
NP_995322.1:p.Ala178Glu
|
|