NM_005585.5:c.1069T>G
MANE Select
|
NP_005576.3:p.Phe357Val
|
ENST00000288840.10:c.1069T>G
MANE Select
|
ENSP00000288840.5:p.Phe357Val
|
NM_005585.4:c.1069T>G
|
NP_005576.3:p.Phe357Val
|
NR_027654.1:n.2124T>G
|
|
NR_027654.2:n.2224T>G
|
|
ENST00000288840.9:c.1069T>G
|
ENSP00000288840.5:p.Phe357Val
|
ENST00000557916.5:c.1201T>G
|
ENSP00000452955.1:n.1201T>G
|
ENST00000559931.5:c.373T>G
|
ENSP00000453446.1:n.373T>G
|
XM_011521561.1:c.286T>G
|
XP_011519863.1:p.Phe96Val
|
XM_011521561.2:c.286T>G
|
XP_011519863.1:p.Phe96Val
|
XR_931825.1:n.2468T>G
|
|