ENST00000335757.10:c.303G>T
MANE Select
|
ENSP00000336888.4:p.Leu101=
|
|
ENST00000335757.9:c.303G>T
|
ENSP00000336888.4:p.Leu101=
|
|
ENST00000407327.8:c.297G>T
|
ENSP00000385135.3:p.Leu99=
|
|
ENST00000586078.5:c.303G>T
|
ENSP00000466664.1:p.Leu101=
|
|
ENST00000588409.1:c.245+3110G>T
|
ENSP00000468070.1:n.245+3110G>T
|
|
ENST00000588465.5:n.212G>T
|
|
|
ENST00000588688.5:c.144G>T
|
ENSP00000467552.1:p.Leu48=
|
|
ENST00000590382.5:c.138G>T
|
ENSP00000468691.1:p.Leu46=
|
|
ENST00000590857.5:c.-247G>T
|
ENSP00000465547.1:n.-247G>T
|
|
ENST00000592293.5:c.*100G>T
|
ENSP00000466612.1:n.*100G>T
|
|
NM_001145056.1:c.297G>T
|
NP_001138528.1:p.Leu99=
|
|
NM_020428.3:c.303G>T
|
NP_065161.3:p.Leu101=
|
|
XM_005259997.1:c.303G>T
|
XP_005260054.1:p.Leu101=
|
|
XM_005259999.1:c.297G>T
|
XP_005260056.1:p.Leu99=
|
|
NM_001363611.1:c.303G>T
|
NP_001350540.1:p.Leu101=
|
|
XM_005259999.2:c.297G>T
|
XP_005260056.1:p.Leu99=
|
|
NM_020428.4:c.303G>T
MANE Select
|
NP_065161.3:p.Leu101=
|
|
NM_001145056.2:c.297G>T
|
NP_001138528.1:p.Leu99=
|
|
NM_001363611.2:c.303G>T
|
NP_001350540.1:p.Leu101=
|
|