ENST00000288840.10:c.968C>G
MANE Select
|
ENSP00000288840.5:p.Pro323Arg
|
|
ENST00000288840.9:c.968C>G
|
ENSP00000288840.5:p.Pro323Arg
|
|
ENST00000557916.5:c.1100C>G
|
ENSP00000452955.1:n.1100C>G
|
|
ENST00000559931.5:c.272C>G
|
ENSP00000453446.1:n.272C>G
|
|
NM_005585.4:c.968C>G
|
NP_005576.3:p.Pro323Arg
|
|
NR_027654.1:n.2023C>G
|
|
|
XM_011521561.1:c.185C>G
|
XP_011519863.1:p.Pro62Arg
|
|
XR_931825.1:n.2367C>G
|
|
|
XM_011521561.2:c.185C>G
|
XP_011519863.1:p.Pro62Arg
|
|
NM_005585.5:c.968C>G
MANE Select
|
NP_005576.3:p.Pro323Arg
|
|
NR_027654.2:n.2123C>G
|
|
|