ENST00000288840.10:c.961A>G
MANE Select
|
ENSP00000288840.5:p.Met321Val
|
|
ENST00000288840.9:c.961A>G
|
ENSP00000288840.5:p.Met321Val
|
|
ENST00000557916.5:c.1093A>G
|
ENSP00000452955.1:n.1093A>G
|
|
ENST00000559931.5:c.265A>G
|
ENSP00000453446.1:n.265A>G
|
|
NM_005585.4:c.961A>G
|
NP_005576.3:p.Met321Val
|
|
NR_027654.1:n.2016A>G
|
|
|
XM_011521561.1:c.178A>G
|
XP_011519863.1:p.Met60Val
|
|
XR_931825.1:n.2360A>G
|
|
|
XM_011521561.2:c.178A>G
|
XP_011519863.1:p.Met60Val
|
|
NM_005585.5:c.961A>G
MANE Select
|
NP_005576.3:p.Met321Val
|
|
NR_027654.2:n.2116A>G
|
|
|