ENST00000409644.6:c.3323T>G
MANE Select
|
ENSP00000386609.1:p.Leu1108Arg
|
|
ENST00000309182.9:c.170T>G
|
ENSP00000312074.5:p.Leu57Arg
|
|
ENST00000409644.5:c.3323T>G
|
ENSP00000386609.1:p.Leu1108Arg
|
|
ENST00000418841.5:c.-89+3496T>G
|
ENSP00000395198.1:n.-89+3496T>G
|
|
ENST00000419248.5:c.-14-2098T>G
|
ENSP00000407845.1:n.-14-2098T>G
|
|
ENST00000437219.6:c.59-2098T>G
|
ENSP00000391074.2:n.59-2098T>G
|
|
ENST00000446363.5:c.-308-2473T>G
|
ENSP00000401560.1:n.-308-2473T>G
|
|
ENST00000455636.5:c.59-2098T>G
|
ENSP00000395226.1:n.59-2098T>G
|
|
ENST00000464528.5:n.709T>G
|
|
|
ENST00000468539.5:c.63-4043T>G
|
ENSP00000460742.1:n.63-4043T>G
|
|
ENST00000492901.1:n.88-2098T>G
|
|
|
ENST00000575206.1:c.73T>G
|
|
|
NM_001163673.1:c.59-2098T>G
|
NP_001157145.1:n.59-2098T>G
|
|
NM_001163809.1:c.3323T>G
|
NP_001157281.1:p.Leu1108Arg
|
|
NM_001163811.1:c.-14-2098T>G
|
NP_001157283.1:n.-14-2098T>G
|
|
NM_152348.3:c.170T>G
|
NP_689561.2:p.Leu57Arg
|
|
XM_005256454.2:c.3323T>G
|
XP_005256511.1:p.Leu1108Arg
|
|
XM_011523650.1:c.3323T>G
|
XP_011521952.1:p.Leu1108Arg
|
|
XM_011523651.1:c.170T>G
|
XP_011521953.1:p.Leu57Arg
|
|
XR_933973.1:n.3467T>G
|
|
|
XM_011523651.2:c.170T>G
|
XP_011521953.1:p.Leu57Arg
|
|
XM_017024184.1:c.3323T>G
|
XP_016879673.1:p.Leu1108Arg
|
|
XR_001752427.1:n.3475T>G
|
|
|
XR_933973.2:n.3475T>G
|
|
|
NM_001163809.2:c.3323T>G
MANE Select
|
NP_001157281.1:p.Leu1108Arg
|
|
NM_001163811.2:c.-14-2098T>G
|
NP_001157283.1:n.-14-2098T>G
|
|
NM_152348.4:c.170T>G
|
NP_689561.2:p.Leu57Arg
|
|
NM_001163673.2:c.59-2098T>G
|
NP_001157145.1:n.59-2098T>G
|
|