ENST00000340855.11:c.406G>C
MANE Select
|
ENSP00000339801.6:p.Val136Leu
|
|
ENST00000651111.1:c.-215-2287G>C
|
ENSP00000498395.1:n.-215-2287G>C
|
|
ENST00000340855.10:c.406G>C
|
ENSP00000339801.6:p.Val136Leu
|
|
ENST00000370441.8:c.406G>C
|
ENSP00000359470.4:p.Val136Leu
|
|
ENST00000422081.6:c.-215-2287G>C
|
ENSP00000477056.1:n.-215-2287G>C
|
|
ENST00000427113.2:n.770-1101G>C
|
|
|
ENST00000428056.6:c.406G>C
|
ENSP00000390241.2:p.Val136Leu
|
|
ENST00000441880.1:n.114-16226G>C
|
|
|
ENST00000464251.5:c.229G>C
|
ENSP00000428980.1:p.Val77Leu
|
|
ENST00000466323.5:c.406G>C
|
ENSP00000418264.1:p.Val136Leu
|
|
ENST00000490775.5:n.65G>C
|
|
|
ENST00000523759.5:n.533-2287G>C
|
|
|
NM_000202.6:c.406G>C
|
NP_000193.1:p.Val136Leu
|
|
NM_001166550.2:c.136G>C
|
NP_001160022.1:p.Val46Leu
|
|
NM_006123.4:c.406G>C
|
NP_006114.1:p.Val136Leu
|
|
NR_104128.1:n.623G>C
|
|
|
NM_000202.7:c.406G>C
|
NP_000193.1:p.Val136Leu
|
|
NM_001166550.3:c.136G>C
|
NP_001160022.1:p.Val46Leu
|
|
NM_000202.8:c.406G>C
MANE Select
|
NP_000193.1:p.Val136Leu
|
|
NM_001166550.4:c.136G>C
|
NP_001160022.1:p.Val46Leu
|
|
NM_006123.5:c.406G>C
|
NP_006114.1:p.Val136Leu
|
|
NR_104128.2:n.575G>C
|
|
|