ENST00000288167.8:c.1414G>T
(IL17RB)
MANE Select
|
ENSP00000288167.3:p.Ala472Ser
|
|
ENST00000288167.7:c.1414G>T
(IL17RB)
|
ENSP00000288167.3:p.Ala472Ser
|
|
ENST00000475124.1:n.2447G>T
(IL17RB)
|
|
|
NM_018725.3:c.1414G>T
(IL17RB)
|
NP_061195.2:p.Ala472Ser
|
|
XM_005265310.3:c.1501G>T
(IL17RB)
|
XP_005265367.1:p.Ala501Ser
|
|
XM_005265311.3:c.1453G>T
(IL17RB)
|
XP_005265368.1:p.Ala485Ser
|
|
XM_005265312.3:c.1366G>T
(IL17RB)
|
XP_005265369.1:p.Ala456Ser
|
|
XM_005265587.3:c.*46-194C>A
(ACTR8)
|
XP_005265644.1:n.*46-194C>A
|
|
XM_011533940.1:c.1150G>T
(IL17RB)
|
XP_011532242.1:p.Ala384Ser
|
|
XR_245147.3:n.1715G>T
(IL17RB)
|
|
|
XR_940467.1:n.1580G>T
(IL17RB)
|
|
|
XR_940468.1:n.1493G>T
(IL17RB)
|
|
|
XM_005265310.5:c.1501G>T
(IL17RB)
|
XP_005265367.1:p.Ala501Ser
|
|
XM_005265311.5:c.1453G>T
(IL17RB)
|
XP_005265368.1:p.Ala485Ser
|
|
XM_005265312.5:c.1366G>T
(IL17RB)
|
XP_005265369.1:p.Ala456Ser
|
|
XM_005265587.5:c.*46-194C>A
(ACTR8)
|
XP_005265644.1:n.*46-194C>A
|
|
XM_011533941.3:c.*294G>T
(IL17RB)
|
XP_011532243.1:n.*294G>T
|
|
XM_011534249.3:c.*3506C>A
(ACTR8)
|
XP_011532551.1:n.*3506C>A
|
|
XM_017006804.2:c.1150G>T
(IL17RB)
|
XP_016862293.1:p.Ala384Ser
|
|
XM_017006805.2:c.1102G>T
(IL17RB)
|
XP_016862294.1:p.Ala368Ser
|
|
XM_017006806.2:c.1063G>T
(IL17RB)
|
XP_016862295.1:p.Ala355Ser
|
|
XM_017006807.2:c.*294G>T
(IL17RB)
|
XP_016862296.1:n.*294G>T
|
|
XR_940516.3:n.5459C>A
(ACTR8)
|
|
|
NM_018725.4:c.1414G>T
(IL17RB)
MANE Select
|
NP_061195.2:p.Ala472Ser
|
|