ENST00000288840.10:c.1110G>C
MANE Select
|
ENSP00000288840.5:p.Gln370His
|
|
ENST00000288840.9:c.1110G>C
|
ENSP00000288840.5:p.Gln370His
|
|
ENST00000557916.5:c.1242G>C
|
ENSP00000452955.1:n.1242G>C
|
|
ENST00000559931.5:c.414G>C
|
ENSP00000453446.1:n.414G>C
|
|
NM_005585.4:c.1110G>C
|
NP_005576.3:p.Gln370His
|
|
NR_027654.1:n.2165G>C
|
|
|
XM_011521561.1:c.327G>C
|
XP_011519863.1:p.Gln109His
|
|
XR_931825.1:n.2509G>C
|
|
|
XM_011521561.2:c.327G>C
|
XP_011519863.1:p.Gln109His
|
|
NM_005585.5:c.1110G>C
MANE Select
|
NP_005576.3:p.Gln370His
|
|
NR_027654.2:n.2265G>C
|
|
|