ENST00000427724.7:c.3518T>G
|
ENSP00000390717.3:p.Leu1173Arg
|
|
ENST00000643257.2:c.3635T>G
MANE Select
|
ENSP00000493815.1:p.Leu1212Arg
|
|
ENST00000650162.1:c.3290T>G
|
ENSP00000497075.1:p.Leu1097Arg
|
|
ENST00000674413.1:c.3034T>G
|
|
|
ENST00000323668.11:c.3401T>G
|
ENSP00000325223.6:p.Leu1134Arg
|
|
ENST00000377797.7:c.3632T>G
|
ENSP00000367028.4:p.Leu1211Arg
|
|
ENST00000427724.6:c.3518T>G
|
ENSP00000390717.2:p.Leu1173Arg
|
|
ENST00000439160.6:c.3521T>G
|
ENSP00000406888.2:p.Leu1174Arg
|
|
ENST00000445265.6:c.3404T>G
|
ENSP00000409944.2:p.Leu1135Arg
|
|
ENST00000504761.6:c.3632T>G
|
ENSP00000421655.2:p.Leu1211Arg
|
|
ENST00000513346.5:c.3632T>G
|
ENSP00000427484.1:p.Leu1211Arg
|
|
ENST00000514442.5:n.3682T>G
|
|
|
ENST00000515516.1:c.343-3340T>G
|
ENSP00000426471.1:n.343-3340T>G
|
|
NM_000356.3:c.3401T>G
|
NP_000347.2:p.Leu1134Arg
|
|
NM_001135243.1:c.3632T>G
|
NP_001128715.1:p.Leu1211Arg
|
|
NM_001135244.1:c.3521T>G
|
NP_001128716.1:p.Leu1174Arg
|
|
NM_001135245.1:c.3404T>G
|
NP_001128717.1:p.Leu1135Arg
|
|
NM_001195141.1:c.3518T>G
|
NP_001182070.1:p.Leu1173Arg
|
|
XM_005268502.2:c.3746T>G
|
XP_005268559.1:p.Leu1249Arg
|
|
XM_005268503.2:c.3743T>G
|
XP_005268560.1:p.Leu1248Arg
|
|
XM_005268504.2:c.3743T>G
|
XP_005268561.1:p.Leu1248Arg
|
|
XM_005268505.2:c.3635T>G
|
XP_005268562.1:p.Leu1212Arg
|
|
XM_005268506.2:c.3632T>G
|
XP_005268563.1:p.Leu1211Arg
|
|
XM_005268507.2:c.3515T>G
|
XP_005268564.1:p.Leu1172Arg
|
|
XM_011537678.1:c.3566T>G
|
XP_011535980.1:p.Leu1189Arg
|
|
XR_427778.1:n.3750T>G
|
|
|
XR_427780.1:n.3639T>G
|
|
|
XM_005268502.4:c.3746T>G
|
XP_005268559.1:p.Leu1249Arg
|
|
XM_005268503.4:c.3743T>G
|
XP_005268560.1:p.Leu1248Arg
|
|
XM_005268504.4:c.3743T>G
|
XP_005268561.1:p.Leu1248Arg
|
|
XM_005268505.4:c.3635T>G
|
XP_005268562.1:p.Leu1212Arg
|
|
XM_005268506.4:c.3632T>G
|
XP_005268563.1:p.Leu1211Arg
|
|
XM_005268507.4:c.3515T>G
|
XP_005268564.1:p.Leu1172Arg
|
|
XM_011537678.3:c.3566T>G
|
XP_011535980.1:p.Leu1189Arg
|
|
XM_017009792.2:c.3629T>G
|
XP_016865281.1:p.Leu1210Arg
|
|
XM_017009793.2:c.3455T>G
|
XP_016865282.1:p.Leu1152Arg
|
|
XM_017009794.2:c.3341T>G
|
XP_016865283.1:p.Leu1114Arg
|
|
XR_427778.3:n.3752T>G
|
|
|
XR_427780.3:n.3641T>G
|
|
|
NM_000356.4:c.3401T>G
|
NP_000347.2:p.Leu1134Arg
|
|
NM_001135244.2:c.3521T>G
|
NP_001128716.1:p.Leu1174Arg
|
|
NM_001135245.2:c.3404T>G
|
NP_001128717.1:p.Leu1135Arg
|
|
NM_001195141.2:c.3518T>G
|
NP_001182070.1:p.Leu1173Arg
|
|
NM_001371623.1:c.3635T>G
MANE Select
|
NP_001358552.1:p.Leu1212Arg
|
|
NM_001135243.2:c.3632T>G
|
NP_001128715.1:p.Leu1211Arg
|
|