ENST00000288840.10:c.1077C>A
MANE Select
|
ENSP00000288840.5:p.Asp359Glu
|
|
ENST00000288840.9:c.1077C>A
|
ENSP00000288840.5:p.Asp359Glu
|
|
ENST00000557916.5:c.1209C>A
|
ENSP00000452955.1:n.1209C>A
|
|
ENST00000559931.5:c.381C>A
|
ENSP00000453446.1:n.381C>A
|
|
NM_005585.4:c.1077C>A
|
NP_005576.3:p.Asp359Glu
|
|
NR_027654.1:n.2132C>A
|
|
|
XM_011521561.1:c.294C>A
|
XP_011519863.1:p.Asp98Glu
|
|
XR_931825.1:n.2476C>A
|
|
|
XM_011521561.2:c.294C>A
|
XP_011519863.1:p.Asp98Glu
|
|
NM_005585.5:c.1077C>A
MANE Select
|
NP_005576.3:p.Asp359Glu
|
|
NR_027654.2:n.2232C>A
|
|
|