ENST00000324001.8:c.*152A>G
MANE Select
|
ENSP00000326018.6:n.*152A>G
|
|
ENST00000673881.1:c.*152A>G
|
ENSP00000501070.1:n.*152A>G
|
|
ENST00000674005.2:c.*152A>G
|
ENSP00000501261.1:n.*152A>G
|
|
ENST00000674773.1:c.*152A>G
|
ENSP00000502579.1:n.*152A>G
|
|
ENST00000676076.1:c.4399A>G
|
|
|
ENST00000676316.1:c.4425A>G
|
|
|
ENST00000291825.11:c.*4743A>G
|
ENSP00000291825.6:n.*4743A>G
|
|
ENST00000324001.7:c.*152A>G
|
ENSP00000326018.6:n.*152A>G
|
|
NM_020956.2:c.*4743A>G , LRG_265t1:c.*4743A>G
|
NP_066007.1:n.*4743A>G
|
|
NM_181882.2:c.*152A>G , LRG_265t2:c.*152A>G
|
NP_870998.2:n.*152A>G
|
|
XM_011527171.1:c.*152A>G
|
XP_011525473.1:n.*152A>G
|
|
XM_011527171.2:c.*152A>G
|
XP_011525473.1:n.*152A>G
|
|
XM_017027046.1:c.*152A>G
|
XP_016882535.1:n.*152A>G
|
|
XM_017027047.1:c.*152A>G
|
XP_016882536.1:n.*152A>G
|
|
NM_181882.3:c.*152A>G
MANE Select
|
NP_870998.2:n.*152A>G
|
|