|
ENST00000218758.10:c.387C>T
(ACP5)
|
ENSP00000218758.4:p.Arg129=
|
|
|
ENST00000412435.7:c.387C>T
(ACP5)
|
ENSP00000392374.1:p.Arg129=
|
|
|
ENST00000588524.6:n.893C>T
(ACP5)
|
|
|
|
ENST00000588625.2:c.512C>T
(ACP5)
|
ENSP00000512197.1:n.512C>T
|
|
|
ENST00000589792.6:c.387C>T
(ACP5)
|
ENSP00000468685.2:p.Arg129=
|
|
|
ENST00000590832.2:c.387C>T
(ACP5)
|
ENSP00000465127.2:p.Arg129=
|
|
|
ENST00000591319.2:c.387C>T
(ACP5)
|
ENSP00000464831.2:p.Arg129=
|
|
|
ENST00000592659.2:c.387C>T
(ACP5)
|
ENSP00000465498.2:p.Arg129=
|
|
|
ENST00000592828.7:c.387C>T
(ACP5)
|
ENSP00000468767.3:p.Arg129=
|
|
|
ENST00000649386.2:c.387C>T
(ACP5)
|
ENSP00000497140.2:p.Arg129=
|
|
|
ENST00000695791.1:c.387C>T
(ACP5)
|
ENSP00000512173.1:p.Arg129=
|
|
|
ENST00000695809.1:c.384C>T
(ACP5)
|
ENSP00000512189.1:p.Arg128=
|
|
|
ENST00000695810.1:c.311+76C>T
(ACP5)
|
ENSP00000512190.1:n.311+76C>T
|
|
|
ENST00000695811.1:c.387C>T
(ACP5)
|
ENSP00000512191.1:p.Arg129=
|
|
|
ENST00000695812.1:n.1005C>T
(ACP5)
|
|
|
|
ENST00000695813.1:c.384C>T
(ACP5)
|
ENSP00000512192.1:p.Arg128=
|
|
|
ENST00000695814.1:c.288C>T
(ACP5)
|
ENSP00000512193.1:p.Arg96=
|
|
|
ENST00000695815.1:c.384C>T
(ACP5)
|
ENSP00000512194.1:p.Arg128=
|
|
|
ENST00000695816.1:n.815C>T
(ACP5)
|
|
|
|
ENST00000695817.1:c.384C>T
(ACP5)
|
ENSP00000512195.1:p.Arg128=
|
|
|
ENST00000695818.1:c.262-130C>T
(ACP5)
|
ENSP00000512196.1:n.262-130C>T
|
|
|
ENST00000695819.1:n.892C>T
(ACP5)
|
|
|
|
ENST00000695820.1:c.311+76C>T
(ACP5)
|
ENSP00000512198.1:n.311+76C>T
|
|
|
ENST00000695821.1:c.311+76C>T
(ACP5)
|
ENSP00000512199.1:n.311+76C>T
|
|
|
ENST00000695838.1:n.2236C>T
(ACP5)
|
|
|
|
ENST00000648477.1:c.387C>T
(ACP5)
MANE Select
|
ENSP00000496973.1:p.Arg129=
|
|
|
ENST00000218758.9:c.387C>T
(ACP5)
|
ENSP00000218758.4:p.Arg129=
|
|
|
ENST00000412435.6:c.387C>T
(ACP5)
|
ENSP00000392374.1:p.Arg129=
|
|
|
ENST00000433365.2:c.387C>T
(ACP5)
|
ENSP00000413456.1:p.Arg129=
|
|
|
ENST00000585493.5:c.-94+1365G>A
(ZNF627)
|
ENSP00000464997.1:n.-94+1365G>A
|
|
|
ENST00000588524.5:n.893C>T
(ACP5)
|
|
|
|
ENST00000588625.1:n.226C>T
(ACP5)
|
|
|
|
ENST00000590420.1:c.54+546C>T
(ACP5)
|
ENSP00000468509.1:n.54+546C>T
|
|
|
ENST00000592828.5:c.387C>T
(ACP5)
|
ENSP00000468767.1:p.Arg129=
|
|
|
ENST00000593279.5:n.519+1365G>A
(ZNF627)
|
|
|
|
NM_001111034.1:c.387C>T
(ACP5)
|
NP_001104504.1:p.Arg129=
|
|
|
NM_001111035.1:c.387C>T
(ACP5)
|
NP_001104505.1:p.Arg129=
|
|
|
NM_001111036.1:c.387C>T
(ACP5)
|
NP_001104506.1:p.Arg129=
|
|
|
NM_001611.3:c.387C>T
(ACP5)
|
NP_001602.1:p.Arg129=
|
|
|
XM_005259938.1:c.387C>T
(ACP5)
|
XP_005259995.1:p.Arg129=
|
|
|
XM_005259939.3:c.387C>T
(ACP5)
|
XP_005259996.1:p.Arg129=
|
|
|
XM_011527780.1:c.-94+1365G>A
(ZNF627)
|
XP_011526082.1:n.-94+1365G>A
|
|
|
XM_011528069.1:c.387C>T
(ACP5)
|
XP_011526371.1:p.Arg129=
|
|
|
NM_001111034.2:c.387C>T
(ACP5)
|
NP_001104504.1:p.Arg129=
|
|
|
NM_001111035.2:c.387C>T
(ACP5)
|
NP_001104505.1:p.Arg129=
|
|
|
NM_001111036.2:c.387C>T
(ACP5)
|
NP_001104506.1:p.Arg129=
|
|
|
NM_001322023.1:c.387C>T
(ACP5)
|
NP_001308952.1:p.Arg129=
|
|
|
NM_001611.5:c.387C>T
(ACP5)
MANE Select
|
NP_001602.1:p.Arg129=
|
|
|
XM_011527780.2:c.-94+1365G>A
(ZNF627)
|
XP_011526082.1:n.-94+1365G>A
|
|
|
XM_011528069.2:c.387C>T
(ACP5)
|
XP_011526371.1:p.Arg129=
|
|
|
NM_001111034.3:c.387C>T
(ACP5)
|
NP_001104504.1:p.Arg129=
|
|
|
NM_001111035.3:c.387C>T
(ACP5)
|
NP_001104505.1:p.Arg129=
|
|
|
NM_001111036.3:c.387C>T
(ACP5)
|
NP_001104506.1:p.Arg129=
|
|
|
NM_001322023.2:c.387C>T
(ACP5)
|
NP_001308952.1:p.Arg129=
|
|
