ENST00000335757.10:c.339G>A
MANE Select
|
ENSP00000336888.4:p.Val113=
|
|
ENST00000335757.9:c.339G>A
|
ENSP00000336888.4:p.Val113=
|
|
ENST00000407327.8:c.333G>A
|
ENSP00000385135.3:p.Val111=
|
|
ENST00000586078.5:c.339G>A
|
ENSP00000466664.1:p.Val113=
|
|
ENST00000588409.1:c.245+3279G>A
|
ENSP00000468070.1:n.245+3279G>A
|
|
ENST00000588465.5:n.248G>A
|
|
|
ENST00000588688.5:c.180G>A
|
ENSP00000467552.1:p.Val60=
|
|
ENST00000590382.5:c.174G>A
|
ENSP00000468691.1:p.Val58=
|
|
ENST00000590857.5:c.-211G>A
|
ENSP00000465547.1:n.-211G>A
|
|
ENST00000592293.5:c.*136G>A
|
ENSP00000466612.1:n.*136G>A
|
|
NM_001145056.1:c.333G>A
|
NP_001138528.1:p.Val111=
|
|
NM_020428.3:c.339G>A
|
NP_065161.3:p.Val113=
|
|
XM_005259997.1:c.339G>A
|
XP_005260054.1:p.Val113=
|
|
XM_005259999.1:c.333G>A
|
XP_005260056.1:p.Val111=
|
|
NM_001363611.1:c.339G>A
|
NP_001350540.1:p.Val113=
|
|
XM_005259999.2:c.333G>A
|
XP_005260056.1:p.Val111=
|
|
NM_020428.4:c.339G>A
MANE Select
|
NP_065161.3:p.Val113=
|
|
NM_001145056.2:c.333G>A
|
NP_001138528.1:p.Val111=
|
|
NM_001363611.2:c.339G>A
|
NP_001350540.1:p.Val113=
|
|