ENST00000288840.10:c.987C>G
MANE Select
|
ENSP00000288840.5:p.Ser329Arg
|
|
ENST00000288840.9:c.987C>G
|
ENSP00000288840.5:p.Ser329Arg
|
|
ENST00000557916.5:c.1119C>G
|
ENSP00000452955.1:n.1119C>G
|
|
ENST00000559931.5:c.291C>G
|
ENSP00000453446.1:n.291C>G
|
|
NM_005585.4:c.987C>G
|
NP_005576.3:p.Ser329Arg
|
|
NR_027654.1:n.2042C>G
|
|
|
XM_011521561.1:c.204C>G
|
XP_011519863.1:p.Ser68Arg
|
|
XR_931825.1:n.2386C>G
|
|
|
XM_011521561.2:c.204C>G
|
XP_011519863.1:p.Ser68Arg
|
|
NM_005585.5:c.987C>G
MANE Select
|
NP_005576.3:p.Ser329Arg
|
|
NR_027654.2:n.2142C>G
|
|
|