ENST00000288840.10:c.1006T>C
MANE Select
|
ENSP00000288840.5:p.Tyr336His
|
|
ENST00000288840.9:c.1006T>C
|
ENSP00000288840.5:p.Tyr336His
|
|
ENST00000557916.5:c.1138T>C
|
ENSP00000452955.1:n.1138T>C
|
|
ENST00000559931.5:c.310T>C
|
ENSP00000453446.1:n.310T>C
|
|
NM_005585.4:c.1006T>C
|
NP_005576.3:p.Tyr336His
|
|
NR_027654.1:n.2061T>C
|
|
|
XM_011521561.1:c.223T>C
|
XP_011519863.1:p.Tyr75His
|
|
XR_931825.1:n.2405T>C
|
|
|
XM_011521561.2:c.223T>C
|
XP_011519863.1:p.Tyr75His
|
|
NM_005585.5:c.1006T>C
MANE Select
|
NP_005576.3:p.Tyr336His
|
|
NR_027654.2:n.2161T>C
|
|
|