|
NM_000426.4:c.9295A>T
MANE Select
|
NP_000417.3:p.Lys3099Ter
|
|
ENST00000421865.3:c.9295A>T
MANE Select
|
ENSP00000400365.2:p.Lys3099Ter
|
|
NM_000426.3:c.9295A>T , LRG_409t1:c.9295A>T
|
NP_000417.2:p.Lys3099Ter
|
|
NM_001079823.1:c.9283A>T
|
NP_001073291.1:p.Lys3095Ter
|
|
NM_001079823.2:c.9283A>T
|
NP_001073291.2:p.Lys3095Ter
|
|
ENST00000421865.2:c.9295A>T
|
ENSP00000400365.2:p.Lys3099Ter
|
|
ENST00000494137.2:c.1360A>T
|
ENSP00000510626.1:p.Lys454Ter
|
|
ENST00000498257.6:c.1360A>T
|
ENSP00000510533.1:p.Lys454Ter
|
|
ENST00000617695.4:c.9283A>T
|
ENSP00000481744.1:p.Lys3095Ter
|
|
ENST00000617695.5:c.9283A>T
|
ENSP00000481744.2:p.Lys3095Ter
|
|
ENST00000618192.4:c.9292A>T
|
ENSP00000480802.1:p.Lys3098Ter
|
|
ENST00000618192.5:c.9559A>T
|
ENSP00000480802.2:p.Lys3187Ter
|
|
ENST00000688198.1:n.2273A>T
|
|
|
ENST00000688799.1:c.1360A>T
|
ENSP00000508458.1:p.Lys454Ter
|
|
ENST00000690858.1:n.4168A>T
|
|
|
ENST00000693461.1:n.1632A>T
|
|
|
XM_005266981.2:c.9559A>T
|
XP_005267038.1:p.Lys3187Ter
|
|
XM_005266981.3:c.9559A>T
|
XP_005267038.1:p.Lys3187Ter
|
|
XM_005266982.2:c.9547A>T
|
XP_005267039.1:p.Lys3183Ter
|
|
XM_005266982.3:c.9547A>T
|
XP_005267039.1:p.Lys3183Ter
|
|
XM_011535820.1:c.9553A>T
|
XP_011534122.1:p.Lys3185Ter
|
|
XM_011535820.2:c.9553A>T
|
XP_011534122.1:p.Lys3185Ter
|
|
XM_017010851.2:c.9565A>T
|
XP_016866340.1:p.Lys3189Ter
|
|
XM_017010852.1:c.7690A>T
|
XP_016866341.1:p.Lys2564Ter
|
|
XR_001743859.1:n.3900+6204T>A
|
|
|
XR_001743860.1:n.1179+6204T>A
|
|
|
XR_001743861.1:n.1346+6204T>A
|
|
|
XR_001743863.1:n.883-13482T>A
|
|
|
XR_002956395.1:n.9131+6204T>A
|
|
|
XR_002956396.1:n.3126+6204T>A
|
|
|
XR_942984.1:n.1460+6204T>A
|
|
|
XR_942985.1:n.1324+6204T>A
|
|