|
NM_004239.4:c.5607A>G
MANE Select
|
NP_004230.2:p.Glu1869=
|
|
ENST00000267622.8:c.5607A>G
MANE Select
|
ENSP00000267622.4:p.Glu1869=
|
|
NM_001321851.1:c.5604A>G
|
NP_001308780.1:p.Glu1868=
|
|
NM_004239.3:c.5607A>G
|
NP_004230.2:p.Glu1869=
|
|
ENST00000554357.5:c.4753A>G
|
|
|
XM_005268214.2:c.4281A>G
|
XP_005268271.1:p.Glu1427=
|
|
XM_005268215.2:c.2577A>G
|
XP_005268272.1:p.Glu859=
|
|
XM_006720321.2:c.5604A>G
|
XP_006720384.1:p.Glu1868=
|
|
XM_017021787.2:c.4902A>G
|
XP_016877276.1:p.Glu1634=
|
|
XM_017021788.2:c.4281A>G
|
XP_016877277.1:p.Glu1427=
|