|
ENST00000218758.10:c.832T>C
(ACP5)
|
ENSP00000218758.4:p.Tyr278His
|
|
|
ENST00000412435.7:c.832T>C
(ACP5)
|
ENSP00000392374.1:p.Tyr278His
|
|
|
ENST00000588524.6:n.1465T>C
(ACP5)
|
|
|
|
ENST00000589792.6:c.832T>C
(ACP5)
|
ENSP00000468685.2:p.Tyr278His
|
|
|
ENST00000590832.2:c.832T>C
(ACP5)
|
ENSP00000465127.2:p.Tyr278His
|
|
|
ENST00000591319.2:c.832T>C
(ACP5)
|
ENSP00000464831.2:p.Tyr278His
|
|
|
ENST00000592659.2:c.832T>C
(ACP5)
|
ENSP00000465498.2:p.Tyr278His
|
|
|
ENST00000592828.7:c.832T>C
(ACP5)
|
ENSP00000468767.3:p.Tyr278His
|
|
|
ENST00000649386.2:c.832T>C
(ACP5)
|
ENSP00000497140.2:p.Tyr278His
|
|
|
ENST00000695791.1:c.832T>C
(ACP5)
|
ENSP00000512173.1:p.Tyr278His
|
|
|
ENST00000695809.1:c.829T>C
(ACP5)
|
ENSP00000512189.1:p.Tyr277His
|
|
|
ENST00000695810.1:c.754T>C
(ACP5)
|
ENSP00000512190.1:p.Tyr252His
|
|
|
ENST00000695811.1:c.832T>C
(ACP5)
|
ENSP00000512191.1:p.Tyr278His
|
|
|
ENST00000695812.1:n.1450T>C
(ACP5)
|
|
|
|
ENST00000695813.1:c.829T>C
(ACP5)
|
ENSP00000512192.1:p.Tyr277His
|
|
|
ENST00000695814.1:c.733T>C
(ACP5)
|
ENSP00000512193.1:p.Tyr245His
|
|
|
ENST00000695815.1:c.829T>C
(ACP5)
|
ENSP00000512194.1:p.Tyr277His
|
|
|
ENST00000695816.1:n.1387T>C
(ACP5)
|
|
|
|
ENST00000695817.1:c.829T>C
(ACP5)
|
ENSP00000512195.1:p.Tyr277His
|
|
|
ENST00000695818.1:c.*335T>C
(ACP5)
|
ENSP00000512196.1:n.*335T>C
|
|
|
ENST00000695819.1:n.1337T>C
(ACP5)
|
|
|
|
ENST00000695820.1:c.754T>C
(ACP5)
|
ENSP00000512198.1:p.Tyr252His
|
|
|
ENST00000695821.1:c.754T>C
(ACP5)
|
ENSP00000512199.1:p.Tyr252His
|
|
|
ENST00000695838.1:n.2808T>C
(ACP5)
|
|
|
|
ENST00000648477.1:c.832T>C
(ACP5)
MANE Select
|
ENSP00000496973.1:p.Tyr278His
|
|
|
ENST00000218758.9:c.832T>C
(ACP5)
|
ENSP00000218758.4:p.Tyr278His
|
|
|
ENST00000412435.6:c.832T>C
(ACP5)
|
ENSP00000392374.1:p.Tyr278His
|
|
|
ENST00000433365.2:c.832T>C
(ACP5)
|
ENSP00000413456.1:p.Tyr278His
|
|
|
ENST00000585493.5:c.-197-94A>G
(ZNF627)
|
ENSP00000464997.1:n.-197-94A>G
|
|
|
ENST00000588651.1:n.428-94A>G
(ZNF627)
|
|
|
|
ENST00000590420.1:c.105T>C
(ACP5)
|
ENSP00000468509.1:p.Ala35=
|
|
|
ENST00000592828.5:c.832T>C
(ACP5)
|
ENSP00000468767.1:p.Tyr278His
|
|
|
ENST00000593279.5:n.416-94A>G
(ZNF627)
|
|
|
|
NM_001111034.1:c.832T>C
(ACP5)
|
NP_001104504.1:p.Tyr278His
|
|
|
NM_001111035.1:c.832T>C
(ACP5)
|
NP_001104505.1:p.Tyr278His
|
|
|
NM_001111036.1:c.832T>C
(ACP5)
|
NP_001104506.1:p.Tyr278His
|
|
|
NM_001611.3:c.832T>C
(ACP5)
|
NP_001602.1:p.Tyr278His
|
|
|
XM_005259938.1:c.832T>C
(ACP5)
|
XP_005259995.1:p.Tyr278His
|
|
|
XM_005259939.3:c.832T>C
(ACP5)
|
XP_005259996.1:p.Tyr278His
|
|
|
XM_011528069.1:c.832T>C
(ACP5)
|
XP_011526371.1:p.Tyr278His
|
|
|
NM_001111034.2:c.832T>C
(ACP5)
|
NP_001104504.1:p.Tyr278His
|
|
|
NM_001111035.2:c.832T>C
(ACP5)
|
NP_001104505.1:p.Tyr278His
|
|
|
NM_001111036.2:c.832T>C
(ACP5)
|
NP_001104506.1:p.Tyr278His
|
|
|
NM_001322023.1:c.832T>C
(ACP5)
|
NP_001308952.1:p.Tyr278His
|
|
|
NM_001611.5:c.832T>C
(ACP5)
MANE Select
|
NP_001602.1:p.Tyr278His
|
|
|
XM_011528069.2:c.832T>C
(ACP5)
|
XP_011526371.1:p.Tyr278His
|
|
|
NM_001111034.3:c.832T>C
(ACP5)
|
NP_001104504.1:p.Tyr278His
|
|
|
NM_001111035.3:c.832T>C
(ACP5)
|
NP_001104505.1:p.Tyr278His
|
|
|
NM_001111036.3:c.832T>C
(ACP5)
|
NP_001104506.1:p.Tyr278His
|
|
|
NM_001322023.2:c.832T>C
(ACP5)
|
NP_001308952.1:p.Tyr278His
|
|
