ENST00000288840.10:c.1082C>A
MANE Select
|
ENSP00000288840.5:p.Pro361His
|
|
ENST00000288840.9:c.1082C>A
|
ENSP00000288840.5:p.Pro361His
|
|
ENST00000557916.5:c.1214C>A
|
ENSP00000452955.1:n.1214C>A
|
|
ENST00000559931.5:c.386C>A
|
ENSP00000453446.1:n.386C>A
|
|
NM_005585.4:c.1082C>A
|
NP_005576.3:p.Pro361His
|
|
NR_027654.1:n.2137C>A
|
|
|
XM_011521561.1:c.299C>A
|
XP_011519863.1:p.Pro100His
|
|
XR_931825.1:n.2481C>A
|
|
|
XM_011521561.2:c.299C>A
|
XP_011519863.1:p.Pro100His
|
|
NM_005585.5:c.1082C>A
MANE Select
|
NP_005576.3:p.Pro361His
|
|
NR_027654.2:n.2237C>A
|
|
|