ENST00000262461.7:c.*138A>G
MANE Select
|
ENSP00000262461.2:n.*138A>G
|
|
ENST00000262461.6:c.*138A>G
|
ENSP00000262461.2:n.*138A>G
|
|
ENST00000343225.4:c.*138A>G
|
ENSP00000340878.4:n.*138A>G
|
|
ENST00000509205.5:c.*390A>G
|
ENSP00000427109.1:n.*390A>G
|
|
NM_001046.2:c.*138A>G
|
NP_001037.1:n.*138A>G
|
|
NM_001256461.1:c.*138A>G
|
NP_001243390.1:n.*138A>G
|
|
NR_046207.1:n.4007A>G
|
|
|
XM_017009771.1:c.*138A>G
|
XP_016865260.1:n.*138A>G
|
|
XR_001742214.1:n.4001A>G
|
|
|
NM_001046.3:c.*138A>G
MANE Select
|
NP_001037.1:n.*138A>G
|
|
NM_001256461.2:c.*138A>G
|
NP_001243390.1:n.*138A>G
|
|
NR_046207.2:n.4032A>G
|
|
|