ENST00000288840.10:c.970G>T
MANE Select
|
ENSP00000288840.5:p.Asp324Tyr
|
|
ENST00000288840.9:c.970G>T
|
ENSP00000288840.5:p.Asp324Tyr
|
|
ENST00000557916.5:c.1102G>T
|
ENSP00000452955.1:n.1102G>T
|
|
ENST00000559931.5:c.274G>T
|
ENSP00000453446.1:n.274G>T
|
|
NM_005585.4:c.970G>T
|
NP_005576.3:p.Asp324Tyr
|
|
NR_027654.1:n.2025G>T
|
|
|
XM_011521561.1:c.187G>T
|
XP_011519863.1:p.Asp63Tyr
|
|
XR_931825.1:n.2369G>T
|
|
|
XM_011521561.2:c.187G>T
|
XP_011519863.1:p.Asp63Tyr
|
|
NM_005585.5:c.970G>T
MANE Select
|
NP_005576.3:p.Asp324Tyr
|
|
NR_027654.2:n.2125G>T
|
|
|